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nstd46 (Campbell et al. 2011)

Organism:
Human
Study Type:
Control Set
Submitter:
Katie Campbell
Description:
Copy number variants (CNVs) can reach appreciable frequencies in the human population, and several of these copy number polymorphisms (CNPs) have been recently associated with human diseases including lupus, psoriasis, Crohn disease, and obesity. Despite new advances, significant biases remain in terms of CNP discovery and genotyping. We developed a novel method based on single channel intensity data and benchmarked against copy numbers determined from sequencing read-depth to successfully obtain CNP genotypes for 1489 CNPs from 487 human DNA samples from diverse ethnic backgrounds. This customized microarray was enriched for segmental duplication-rich regions and novel insertions of sequences not represented in the reference genome assembly or on standard single nucleotide polymorphism (SNP) microarray platforms. We observe that CNPs in segmental duplications are more likely to be population differentiated than CNPs in unique regions (p = 0.015) and that bi-allelic CNPs show greater stratification when compared to frequency-matched SNPs (p = 0.0026). Although bi-allelic CNPs show a strong correlation of copy number with flanking SNP genotypes, the majority of multi-copy CNPs do not (40% with r >0.8). We selected a subset of CNPs for further characterization in 1873 additional samples from 62 populations; this revealed striking population-differentiated structural variants in genes of clinical significance such as the OCLN gene, a tight junction protein involved in hepatitis C viral entry. Our new microarray design allows these variants to be rapidly tested for disease association and our results suggest that CNPs (especially those not in linkage disequilibrium with SNPs) may have contributed disproportionately to human diversity and selection. See Variant Summary counts for nstd46 in dbVar Variant Summary.
Publication(s):
Campbell et al. 2011

Detailed Information: Download 1183 Variant Regions, Download 227380 Variant Calls, Download Both, FTP

Variant Summary

Assembly used for analysis:
Remapped: GRCh38.p12 (hg38)
Remapped: GRCh37.p13 (hg19)
Submitted: NCBI36 (hg18)

Sequence IDChrNumber of Variant RegionsNumber of Variant CallsPlacement typeLink to graphical display
NC_000001.11Chr18617,390RemappedNC_000001.11
NC_000002.12Chr29416,475RemappedNC_000002.12
NC_000003.12Chr37612,328RemappedNC_000003.12
NC_000004.12Chr410014,200RemappedNC_000004.12
NC_000005.10Chr56210,988RemappedNC_000005.10
NC_000006.12Chr67413,196RemappedNC_000006.12
NC_000007.14Chr76812,288RemappedNC_000007.14
NC_000008.11Chr89217,874RemappedNC_000008.11
NC_000009.12Chr9437,375RemappedNC_000009.12
NC_000010.11Chr105010,071RemappedNC_000010.11
NC_000011.10Chr11538,262RemappedNC_000011.10
NC_000012.12Chr12457,343RemappedNC_000012.12
NC_000013.11Chr13305,332RemappedNC_000013.11
NC_000014.9Chr144210,700RemappedNC_000014.9
NC_000015.10Chr15326,922RemappedNC_000015.10
NC_000016.10Chr16327,668RemappedNC_000016.10
NC_000017.11Chr17359,363RemappedNC_000017.11
NC_000018.10Chr18274,068RemappedNC_000018.10
NC_000019.10Chr19194,882RemappedNC_000019.10
NC_000020.11Chr20183,344RemappedNC_000020.11
NC_000021.9Chr2110938RemappedNC_000021.9
NC_000022.11Chr22144,328RemappedNC_000022.11
NC_000023.11ChrX6418,539RemappedNC_000023.11
NC_000024.10ChrY8570RemappedNC_000024.10
NT_187518.1Chr1|NT_187518.11167RemappedNT_187518.1
NT_187646.1Chr1|NT_187646.11167RemappedNT_187646.1
NW_011332687.1Chr1|NW_011332687.1111RemappedNW_011332687.1
NW_017852928.1Chr1|NW_017852928.12562RemappedNW_017852928.1
NW_018654707.1Chr1|NW_018654707.12520RemappedNW_018654707.1
NT_187523.1Chr2|NT_187523.12496RemappedNT_187523.1
NT_187528.1Chr2|NT_187528.11488RemappedNT_187528.1
NT_187529.1Chr2|NT_187529.11488RemappedNT_187529.1
NT_187530.1Chr2|NT_187530.116RemappedNT_187530.1
NT_187647.1Chr2|NT_187647.12496RemappedNT_187647.1
NW_012132915.1Chr2|NW_012132915.11244RemappedNW_012132915.1
NT_187678.1Chr3|NT_187678.12966RemappedNT_187678.1
NT_187688.1Chr3|NT_187688.11478RemappedNT_187688.1
NT_187689.1Chr3|NT_187689.11478RemappedNT_187689.1
NT_187690.1Chr3|NT_187690.11478RemappedNT_187690.1
NT_187691.1Chr3|NT_187691.11478RemappedNT_187691.1
NT_187532.1Chr3|NT_187532.11478RemappedNT_187532.1
NT_187536.1Chr3|NT_187536.1136RemappedNT_187536.1
NT_187649.1Chr3|NT_187649.11478RemappedNT_187649.1
NT_187545.1Chr4|NT_187545.11488RemappedNT_187545.1
NW_003315915.1Chr4|NW_003315915.11159RemappedNW_003315915.1
NT_187651.1Chr5|NT_187651.12821RemappedNT_187651.1
NT_167246.2Chr6|NT_167246.241,120RemappedNT_167246.2
NT_167247.2Chr6|NT_167247.22840RemappedNT_167247.2
NT_167249.2Chr6|NT_167249.272,415RemappedNT_167249.2
NT_167245.2Chr6|NT_167245.231,311RemappedNT_167245.2
NT_187558.1Chr7|NT_187558.1154RemappedNT_187558.1
NT_187560.1Chr7|NT_187560.11488RemappedNT_187560.1
NT_187562.1Chr7|NT_187562.13968RemappedNT_187562.1
NT_187653.1Chr7|NT_187653.1154RemappedNT_187653.1
NW_018654714.1Chr7|NW_018654714.11207RemappedNW_018654714.1
NW_018654715.1Chr7|NW_018654715.12976RemappedNW_018654715.1
NT_187570.1Chr8|NT_187570.131,375RemappedNT_187570.1
NT_187576.1Chr8|NT_187576.14672RemappedNT_187576.1
NW_018654717.1Chr8|NW_018654717.193,684RemappedNW_018654717.1
NW_003315931.1Chr9|NW_003315931.11488RemappedNW_003315931.1
NW_003315934.1Chr10|NW_003315934.11112RemappedNW_003315934.1
NW_013171806.1Chr10|NW_013171806.12223RemappedNW_013171806.1
NT_187581.1Chr11|NT_187581.11488RemappedNT_187581.1
NT_187583.1Chr11|NT_187583.11119RemappedNT_187583.1
NW_011332695.1Chr11|NW_011332695.11119RemappedNW_011332695.1
NW_019805495.1Chr11|NW_019805495.1146RemappedNW_019805495.1
NT_187658.1Chr12|NT_187658.12487RemappedNT_187658.1
NT_187587.1Chr12|NT_187587.12524RemappedNT_187587.1
NW_003315940.1Chr12|NW_003315940.11486RemappedNW_003315940.1
NW_003571050.1Chr12|NW_003571050.1166RemappedNW_003571050.1
NW_011332696.1Chr12|NW_011332696.1126RemappedNW_011332696.1
NW_018654718.1Chr12|NW_018654718.1123RemappedNW_018654718.1
NW_019805499.1Chr12|NW_019805499.1112RemappedNW_019805499.1
NT_187600.1Chr14|NT_187600.14917RemappedNT_187600.1
NT_187660.1Chr15|NT_187660.1174RemappedNT_187660.1
NW_011332701.1Chr15|NW_011332701.1174RemappedNW_011332701.1
NT_187607.1Chr16|NT_187607.1113RemappedNT_187607.1
NT_187661.1Chr17|NT_187661.141,603RemappedNT_187661.1
NT_187663.1Chr17|NT_187663.11118RemappedNT_187663.1
NW_003871093.1Chr17|NW_003871093.11400RemappedNW_003871093.1
NT_187614.1Chr17|NT_187614.141,304RemappedNT_187614.1
NW_003315953.2Chr17|NW_003315953.2153RemappedNW_003315953.2
NW_003871092.1Chr17|NW_003871092.11109RemappedNW_003871092.1
NW_017363819.1Chr17|NW_017363819.11377RemappedNW_017363819.1
NT_187666.1Chr18|NT_187666.11488RemappedNT_187666.1
NW_003315961.1Chr18|NW_003315961.11488RemappedNW_003315961.1
NT_187693.1Chr19|NT_187693.12732RemappedNT_187693.1
NW_003571060.1Chr19|NW_003571060.11244RemappedNW_003571060.1
NW_003571054.1Chr19|NW_003571054.11244RemappedNW_003571054.1
NT_187623.1Chr20|NT_187623.11488RemappedNT_187623.1
NT_187624.1Chr20|NT_187624.11488RemappedNT_187624.1
NW_003315968.2Chr21|NW_003315968.2168RemappedNW_003315968.2
NT_187629.1Chr22|NT_187629.11436RemappedNT_187629.1
NT_187632.1Chr22|NT_187632.11488RemappedNT_187632.1
NT_187633.1Chr22|NT_187633.11272RemappedNT_187633.1
NW_003315972.2Chr22|NW_003315972.21140RemappedNW_003315972.2
Sequence IDChrNumber of Variant RegionsNumber of Variant CallsPlacement typeLink to graphical display
NC_000001.10Chr18516,902RemappedNC_000001.10
NC_000002.11Chr29516,796RemappedNC_000002.11
NC_000003.11Chr37612,328RemappedNC_000003.11
NC_000004.11Chr410014,200RemappedNC_000004.11
NC_000005.9Chr56210,988RemappedNC_000005.9
NC_000006.11Chr67413,196RemappedNC_000006.11
NC_000007.13Chr76812,288RemappedNC_000007.13
NC_000008.10Chr89318,036RemappedNC_000008.10
NC_000009.11Chr9437,375RemappedNC_000009.11
NC_000010.10Chr105010,071RemappedNC_000010.10
NC_000011.9Chr11538,262RemappedNC_000011.9
NC_000012.11Chr12457,343RemappedNC_000012.11
NC_000013.10Chr13305,332RemappedNC_000013.10
NC_000014.8Chr144310,919RemappedNC_000014.8
NC_000015.9Chr15326,922RemappedNC_000015.9
NC_000016.9Chr16327,668RemappedNC_000016.9
NC_000017.10Chr17369,470RemappedNC_000017.10
NC_000018.9Chr18284,556RemappedNC_000018.9
NC_000019.9Chr19194,882RemappedNC_000019.9
NC_000020.10Chr20183,344RemappedNC_000020.10
NC_000021.8Chr2110938RemappedNC_000021.8
NC_000022.10Chr22154,600RemappedNC_000022.10
NC_000023.10ChrX6418,539RemappedNC_000023.10
NC_000024.9ChrY8570RemappedNC_000024.9
NW_003315903.1Chr1|NW_003315903.11111RemappedNW_003315903.1
NW_003871056.3Chr1|NW_003871056.31488RemappedNW_003871056.3
NW_003315915.1Chr4|NW_003315915.11159RemappedNW_003315915.1
NW_004775427.1Chr4|NW_004775427.11488RemappedNW_004775427.1
NW_004775428.1Chr5|NW_004775428.1180RemappedNW_004775428.1
NT_167245.1Chr6|NT_167245.131,311RemappedNT_167245.1
NT_167246.1Chr6|NT_167246.141,120RemappedNT_167246.1
NT_167247.1Chr6|NT_167247.12840RemappedNT_167247.1
NT_167249.1Chr6|NT_167249.172,415RemappedNT_167249.1
NW_004070866.1Chr6|NW_004070866.11488RemappedNW_004070866.1
NW_003571040.1Chr7|NW_003571040.13968RemappedNW_003571040.1
NW_003571042.1Chr8|NW_003571042.14672RemappedNW_003571042.1
NW_003315931.1Chr9|NW_003315931.11488RemappedNW_003315931.1
NW_004070869.1Chr9|NW_004070869.1159RemappedNW_004070869.1
NW_003315934.1Chr10|NW_003315934.11112RemappedNW_003315934.1
NW_004504302.1Chr10|NW_004504302.11488RemappedNW_004504302.1
NW_003315940.1Chr12|NW_003315940.11486RemappedNW_003315940.1
NW_004166863.1Chr14|NW_004166863.151,199RemappedNW_004166863.1
NT_167251.1Chr17|NT_167251.11313RemappedNT_167251.1
NW_003315949.1Chr17|NW_003315949.131,156RemappedNW_003315949.1
NW_003315953.1Chr17|NW_003315953.1153RemappedNW_003315953.1
NW_003871086.1Chr17|NW_003871086.11118RemappedNW_003871086.1
NW_003871092.1Chr17|NW_003871092.11109RemappedNW_003871092.1
NW_003871093.1Chr17|NW_003871093.11400RemappedNW_003871093.1
NW_004070872.2Chr17|NW_004070872.21488RemappedNW_004070872.2
NW_003571053.2Chr19|NW_003571053.2193RemappedNW_003571053.2
NW_003871094.1Chr19|NW_003871094.11488RemappedNW_003871094.1
NW_004166865.1Chr19|NW_004166865.11488RemappedNW_004166865.1
NW_003315968.1Chr21|NW_003315968.1168RemappedNW_003315968.1
NW_003315972.1Chr22|NW_003315972.11140RemappedNW_003315972.1
NW_003871100.1ChrX|NW_003871100.11254RemappedNW_003871100.1
NW_003871103.3ChrX|NW_003871103.32889RemappedNW_003871103.3
NW_004070877.1ChrX|NW_004070877.11269RemappedNW_004070877.1
NW_004070880.2ChrX|NW_004070880.262,204RemappedNW_004070880.2
NW_004070881.1ChrX|NW_004070881.11259RemappedNW_004070881.1
NW_004070888.1ChrX|NW_004070888.11488RemappedNW_004070888.1
NW_004070890.2ChrX|NW_004070890.261,369RemappedNW_004070890.2
Sequence IDChrNumber of Variant RegionsNumber of Variant CallsPlacement typeLink to graphical display
NC_000001.9Chr18617,390SubmittedNC_000001.9
NC_000002.10Chr29516,796SubmittedNC_000002.10
NC_000003.10Chr37612,328SubmittedNC_000003.10
NC_000004.10Chr410014,200SubmittedNC_000004.10
NC_000005.8Chr56210,988SubmittedNC_000005.8
NC_000006.10Chr67413,196SubmittedNC_000006.10
NC_000007.12Chr76912,679SubmittedNC_000007.12
NC_000008.9Chr89318,036SubmittedNC_000008.9
NC_000009.10Chr9437,375SubmittedNC_000009.10
NC_000010.9Chr105010,071SubmittedNC_000010.9
NC_000011.8Chr11538,262SubmittedNC_000011.8
NC_000012.10Chr12457,343SubmittedNC_000012.10
NC_000013.9Chr13305,332SubmittedNC_000013.9
NC_000014.7Chr144310,919SubmittedNC_000014.7
NC_000015.8Chr15326,922SubmittedNC_000015.8
NC_000016.8Chr16327,668SubmittedNC_000016.8
NC_000017.9Chr17379,958SubmittedNC_000017.9
NC_000018.8Chr18284,556SubmittedNC_000018.8
NC_000019.8Chr19205,370SubmittedNC_000019.8
NC_000020.9Chr20183,344SubmittedNC_000020.9
NC_000021.7Chr2110938SubmittedNC_000021.7
NC_000022.9Chr22154,600SubmittedNC_000022.9
NC_000023.9ChrX6418,539SubmittedNC_000023.9
NC_000024.8ChrY8570SubmittedNC_000024.8

Variant Region remap statusVariant Call remap status
Sequence IDChrVariant Regions on sourcePerfectGoodPassFailMultVariant Calls on sourcePerfectGoodPassFailMult
NC_000001.9Chr18684010117,39016,79104880111
NC_000002.10Chr29595000016,79616,7960000
NC_000003.10Chr37675100012,32811,850478000
NC_000004.10Chr410098000214,20013,553000647
NC_000005.8Chr56259110110,9889,945475488080
NC_000006.10Chr67465000913,19610,1190003,077
NC_000007.12Chr76965110212,67911,5043912070577
NC_000008.9Chr89388100418,03616,87648800672
NC_000009.10Chr9434100027,3756,828000547
NC_000010.9Chr105047100210,0718,98348800600
NC_000011.8Chr11535300008,2628,2620000
NC_000012.10Chr12454400017,3436,857000486
NC_000013.9Chr13303000005,3325,3320000
NC_000014.7Chr144338000510,9199,7200001,199
NC_000015.8Chr15323110006,9226,434488000
NC_000016.8Chr16323200007,6687,6680000
NC_000017.9Chr17372900089,9587,8090002,149
NC_000018.8Chr18282800004,5564,5560000
NC_000019.8Chr19201710025,3704,30148800581
NC_000020.9Chr20181800003,3443,3440000
NC_000021.7Chr21109000193887000068
NC_000022.9Chr22151400014,6004,460000140
NC_000023.9ChrX64441101818,53912,08223748805,732
NC_000024.8ChrY8800005705700000
Variant Region remap statusVariant Call remap status
Sequence IDChrVariant Regions on sourcePerfectGoodPassFailMultVariant Calls on sourcePerfectGoodPassFailMult
NC_000001.9Chr18678200617,39015,356774001,260
NC_000002.10Chr29585301616,79614,59216103211,722
NC_000003.10Chr37673000312,32811,3260001,002
NC_000004.10Chr410098000214,20013,553000647
NC_000005.8Chr56258110210,9889,2044754880821
NC_000006.10Chr67465010813,19610,119048802,589
NC_000007.12Chr76961100712,6799,986391002,302
NC_000008.9Chr893790001418,03612,8760005,160
NC_000009.10Chr9433912017,3755,8404885590488
NC_000010.9Chr105046100310,0719,24848800335
NC_000011.8Chr11534910038,2627,5654400653
NC_000012.10Chr12453700087,3435,7850001,558
NC_000013.9Chr13303000005,3325,3320000
NC_000014.7Chr144336201410,9199,4493340219917
NC_000015.8Chr15323100016,9226,84800074
NC_000016.8Chr16323100017,6687,65500013
NC_000017.9Chr17372900089,9587,7450002,213
NC_000018.8Chr18282600114,5563,58000488488
NC_000019.8Chr19201810015,3704,63848800244
NC_000020.9Chr20181600023,3442,368000976
NC_000021.7Chr21109000193887000068
NC_000022.9Chr22151110034,6003,51125001,064
NC_000023.9ChrX64521020018,53913,8893,67497600
NC_000024.8ChrY8800005705700000

Samplesets

Number of Samplesets: 3

Sampleset ID:
1
Name:
Initial Samples for Analysis
Description:
Samples from five HapMap populations: Utah residents with Northwest European ancestry (CEU), Han Chinese from Beijing (CHB), Japanese from Tokyo (JPT), Maasai from Kinyawa, Kenya (MKK), and Yoruba from Ibadan, Nigeria (YRI)
Size:
487
Organisms:
Homo sapiens
Sampleset Phenotype(s):
None reported
  • Download Samples as CSV file
  • Samples for sampleset 1 (displaying 100 of the 487 samples)
    Sample IDCell TypeSubject ID SexEthnicitySubject AgeSubject Phenotype
    NA10836B-LymphocyteNA10836FemaleUTAH/MORMON44 YearsNot reported
    NA07348B-LymphocyteNA07348FemaleUTAH/MORMON45 YearsNot reported
    NA11993B-LymphocyteNA11993FemaleUTAH/MORMON80 YearsNot reported
    NA10843B-LymphocyteNA10843FemaleUTAH/MORMON49 YearsNot reported
    NA12154B-LymphocyteNA12154MaleUTAH/MORMON92 YearsNot reported
    NA10857B-LymphocyteNA10857MaleUTAH/MORMON47 YearsNot reported
    NA11839B-LymphocyteNA11839MaleUTAH/MORMON67 YearsNot reported
    NA12156B-LymphocyteNA12156FemaleUTAH/MORMON81 YearsNot reported
    NA11881B-LymphocyteNA11881MaleUTAH/MORMON62 YearsNot reported
    NA12335B-LymphocyteNA12335MaleUTAH/MORMONNot reported
    NA11831B-LymphocyteNA11831MaleUTAH/MORMON73 YearsNot reported
    NA10830B-LymphocyteNA10830MaleUTAH/MORMON66 YearsNot reported
    NA06993B-LymphocyteNA06993MaleUTAH/MORMON74 YearsNot reported
    NA07014B-LymphocyteNA07014FemaleUTAH/MORMON39 YearsNot reported
    NA10856B-LymphocyteNA10856MaleUTAH/MORMON46 YearsNot reported
    NA10840B-LymphocyteNA10840FemaleUTAH/MORMON42 YearsNot reported
    NA07048B-LymphocyteNA07048MaleUTAH/MORMON43 YearsNot reported
    NA12056B-LymphocyteNA12056MaleUTAH/MORMON79 YearsNot reported
    NA12236B-LymphocyteNA12236FemaleUTAH/MORMON86 YearsNot reported
    NA12275B-LymphocyteNA12275FemaleUTAH/MORMON69 YearsNot reported
    NA10845B-LymphocyteNA10845MaleUTAH/MORMON49 YearsNot reported
    NA12155B-LymphocyteNA12155MaleUTAH/MORMON86 YearsNot reported
    NA06995B-LymphocyteNA06995MaleUTAH/MORMON45 YearsNot reported
    NA12146B-LymphocyteNA12146MaleUTAH/MORMON61 YearsNot reported
    NA11917B-LymphocyteNA11917MaleUTAH/MORMON66 YearsNot reported
    NA12286B-LymphocyteNA12286MaleUTAH/MORMON70 YearsNot reported
    NA11920B-LymphocyteNA11920FemaleUTAH/MORMON66 YearsNot reported
    NA12249B-LymphocyteNA12249FemaleUTAH/MORMON77 YearsNot reported
    NA11830B-LymphocyteNA11830FemaleUTAH/MORMON63 YearsNot reported
    NA10837B-LymphocyteNA10837MaleUTAH/MORMON43 YearsNot reported
    NA10859B-LymphocyteNA10859FemaleUTAH/MORMON41 YearsNot reported
    NA10838B-LymphocyteNA10838MaleUTAH/MORMON60 YearsNot reported
    NA06991B-LymphocyteNA06991FemaleUTAH/MORMON42 YearsNot reported
    NA11843B-LymphocyteNA11843MaleUTAH/MORMON77 YearsNot reported
    NA11995B-LymphocyteNA11995FemaleUTAH/MORMON84 YearsNot reported
    NA12336B-LymphocyteNA12336FemaleUTAH/MORMONNot reported
    NA06989B-LymphocyteNA06989FemaleUTAH/MORMON62 YearsNot reported
    NA10831B-LymphocyteNA10831FemaleUTAH/MORMON59 YearsNot reported
    NA11894B-LymphocyteNA11894FemaleUTAH/MORMON69 YearsNot reported
    NA11829B-LymphocyteNA11829MaleUTAH/MORMON72 YearsNot reported
    NA11992B-LymphocyteNA11992MaleUTAH/MORMON86 YearsNot reported
    NA10850B-LymphocyteNA10850FemaleUTAH/MORMON48 YearsNot reported
    NA12043B-LymphocyteNA12043MaleUTAH/MORMON74 YearsNot reported
    NA07022B-LymphocyteNA07022MaleUTAH/MORMON63 YearsNot reported
    NA12329B-LymphocyteNA12329FemaleUTAH/MORMONNot reported
    NA06984B-LymphocyteNA06984MaleUTAH/MORMON63 YearsNot reported
    NA10860B-LymphocyteNA10860MaleUTAH/MORMON50 YearsNot reported
    NA06985B-LymphocyteNA06985FemaleUTAH/MORMON69 YearsNot reported
    NA12044B-LymphocyteNA12044FemaleUTAH/MORMON70 YearsNot reported
    NA10852B-LymphocyteNA10852FemaleUTAH/MORMON48 YearsNot reported
    NA12264B-LymphocyteNA12264MaleUTAH/MORMON72 YearsNot reported
    NA12234B-LymphocyteNA12234FemaleUTAH/MORMON74 YearsNot reported
    NA12145B-LymphocyteNA12145FemaleUTAH/MORMON70 YearsNot reported
    NA10851B-LymphocyteNA10851MaleUTAH/MORMON52 YearsNot reported
    NA12004B-LymphocyteNA12004FemaleUTAH/MORMON92 YearsNot reported
    NA07347B-LymphocyteNA07347MaleUTAH/MORMON86 YearsNot reported
    NA07357B-LymphocyteNA07357MaleUTAH/MORMON69 YearsNot reported
    NA12272B-LymphocyteNA12272MaleUTAH/MORMON73 YearsNot reported
    NA12341B-LymphocyteNA12341FemaleUTAH/MORMONNot reported
    NA12283B-LymphocyteNA12283FemaleUTAH/MORMON64 YearsNot reported
    NA06994B-LymphocyteNA06994MaleUTAH/MORMON68 YearsNot reported
    NA07349B-LymphocyteNA07349MaleUTAH/MORMON49 YearsNot reported
    NA11919B-LymphocyteNA11919MaleUTAH/MORMON67 YearsNot reported
    NA11930B-LymphocyteNA11930MaleUTAH/MORMONNot reported
    NA11840B-LymphocyteNA11840FemaleUTAH/MORMON67 YearsNot reported
    NA12282B-LymphocyteNA12282MaleUTAH/MORMON69 YearsNot reported
    NA07051B-LymphocyteNA07051MaleUTAH/MORMON67 YearsNot reported
    NA10864B-LymphocyteNA10864FemaleUTAH/MORMON40 YearsNot reported
    NA11892B-LymphocyteNA11892FemaleUTAH/MORMON73 YearsNot reported
    NA07034B-LymphocyteNA07034MaleUTAH/MORMON71 YearsNot reported
    NA11918B-LymphocyteNA11918FemaleUTAH/MORMON64 YearsNot reported
    NA12248B-LymphocyteNA12248MaleUTAH/MORMON89 YearsNot reported
    NA11994B-LymphocyteNA11994MaleUTAH/MORMON80 YearsNot reported
    NA07031B-LymphocyteNA07031FemaleUTAH/MORMON63 YearsNot reported
    NA12005B-LymphocyteNA12005MaleUTAH/MORMON77 YearsNot reported
    NA11893B-LymphocyteNA11893MaleUTAH/MORMON71 YearsNot reported
    NA06986B-LymphocyteNA06986MaleUTAH/MORMON74 YearsNot reported
    NA10839B-LymphocyteNA10839FemaleUTAH/MORMON55 YearsNot reported
    NA10847B-LymphocyteNA10847FemaleUTAH/MORMON38 YearsNot reported
    NA12287B-LymphocyteNA12287FemaleUTAH/MORMON69 YearsNot reported
    NA12058B-LymphocyteNA12058FemaleUTAH/MORMON81 YearsNot reported
    NA12144B-LymphocyteNA12144MaleUTAH/MORMON71 YearsNot reported
    NA12045B-LymphocyteNA12045MaleUTAH/MORMON74 YearsNot reported
    NA07055B-LymphocyteNA07055FemaleUTAH/MORMON70 YearsNot reported
    NA10855B-LymphocyteNA10855FemaleUTAH/MORMON37 YearsNot reported
    NA10863B-LymphocyteNA10863FemaleUTAH/MORMON43 YearsNot reported
    NA07435B-LymphocyteNA07435MaleUTAH/MORMON77 YearsNot reported
    NA11882B-LymphocyteNA11882FemaleUTAH/MORMON61 YearsNot reported
    NA07346B-LymphocyteNA07346FemaleUTAH/MORMON85 YearsNot reported
    NA07019B-LymphocyteNA07019FemaleUTAH/MORMON45 YearsNot reported
    NA10835B-LymphocyteNA10835MaleUTAH/MORMON39 YearsNot reported
    NA12274B-LymphocyteNA12274MaleUTAH/MORMON72 YearsNot reported
    NA12273B-LymphocyteNA12273FemaleUTAH/MORMON71 YearsNot reported
    NA07037B-LymphocyteNA07037FemaleUTAH/MORMON65 YearsNot reported
    NA07056B-LymphocyteNA07056FemaleUTAH/MORMON65 YearsNot reported
    NA12340B-LymphocyteNA12340MaleUTAH/MORMONNot reported
    NA10846B-LymphocyteNA10846MaleUTAH/MORMON43 YearsNot reported
    NA07000B-LymphocyteNA07000FemaleUTAH/MORMON66 YearsNot reported
    NA12239B-LymphocyteNA12239FemaleUTAH/MORMON61 YearsNot reported
    NA11832B-LymphocyteNA11832FemaleUTAH/MORMON58 YearsNot reported
    Sampleset ID:
    2
    Name:
    Follow-up samples (arrayCGH)
    Description:
    Samples used for follow-up of variants identified in initial samples. These samples are from the following populations: Utah residents with Northwest European ancestry (CEU), Han Chinese from Beijing (CHB), Japanese from Tokyo (JPT), Maasai from Kinyawa, Kenya (MKK), Yoruba from Ibadan, Nigeria (YRI), African American from Southwest USA (ASW), Luhya from Webuye, Kenya (LWK), Mexican American from Los Angeles, CA (MEX), Toscani from Italy (TSI), British from England and Scotland (GBR), Finnish from Finland (FIN), and Han Chinese from South China (CHS)
    Size:
    947
    Organisms:
    Homo sapiens
    Sampleset Phenotype(s):
    None reported
  • Download Samples as CSV file
  • Samples for sampleset 2 (displaying 100 of the 947 samples)
    Sample IDCell TypeSubject ID SexEthnicitySubject Phenotype
    HG00126B-LymphocyteHG00126MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00244B-LymphocyteHG00244MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00114B-LymphocyteHG00114MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00173B-LymphocyteHG00173FemaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00135B-LymphocyteHG00135FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00234B-LymphocyteHG00234MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00150B-LymphocyteHG00150FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00256B-LymphocyteHG00256MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00179B-LymphocyteHG00179FemaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00255B-LymphocyteHG00255FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00152B-LymphocyteHG00152MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00115B-LymphocyteHG00115MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00236B-LymphocyteHG00236FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00148B-LymphocyteHG00148MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00235B-LymphocyteHG00235FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00257B-LymphocyteHG00257FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00113B-LymphocyteHG00113MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00188B-LymphocyteHG00188MaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00185B-LymphocyteHG00185MaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00262B-LymphocyteHG00262FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00157B-LymphocyteHG00157MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00133B-LymphocyteHG00133FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00259B-LymphocyteHG00259FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00177B-LymphocyteHG00177FemaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00231B-LymphocyteHG00231FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00130B-LymphocyteHG00130FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00127B-LymphocyteHG00127FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00176B-LymphocyteHG00176FemaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00112B-LymphocyteHG00112MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00258B-LymphocyteHG00258FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00247B-LymphocyteHG00247FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00186B-LymphocyteHG00186MaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00181B-LymphocyteHG00181MaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00121B-LymphocyteHG00121FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00124B-LymphocyteHG00124FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00253B-LymphocyteHG00253FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00142B-LymphocyteHG00142MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00254B-LymphocyteHG00254FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00134B-LymphocyteHG00134FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00105B-LymphocyteHG00105MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00250B-LymphocyteHG00250FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00249B-LymphocyteHG00249FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00120B-LymphocyteHG00120FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00138B-LymphocyteHG00138MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00103B-LymphocyteHG00103MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00141B-LymphocyteHG00141MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00240B-LymphocyteHG00240FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00143B-LymphocyteHG00143MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00187B-LymphocyteHG00187MaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00145B-LymphocyteHG00145MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00137B-LymphocyteHG00137FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00132B-LymphocyteHG00132FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00178B-LymphocyteHG00178FemaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00118B-LymphocyteHG00118FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00260B-LymphocyteHG00260MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00116B-LymphocyteHG00116MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00243B-LymphocyteHG00243MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00261B-LymphocyteHG00261FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00102B-LymphocyteHG00102FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00245B-LymphocyteHG00245FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00140B-LymphocyteHG00140MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00107B-LymphocyteHG00107MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00264B-LymphocyteHG00264MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00104B-LymphocyteHG00104FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00242B-LymphocyteHG00242MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00190B-LymphocyteHG00190MaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00238B-LymphocyteHG00238FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00128B-LymphocyteHG00128FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00117B-LymphocyteHG00117MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00156B-LymphocyteHG00156MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00263B-LymphocyteHG00263FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00180B-LymphocyteHG00180FemaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00237B-LymphocyteHG00237FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00129B-LymphocyteHG00129MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00123B-LymphocyteHG00123FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00246B-LymphocyteHG00246MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00139B-LymphocyteHG00139MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00183B-LymphocyteHG00183MaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00160B-LymphocyteHG00160MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00159B-LymphocyteHG00159MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00109B-LymphocyteHG00109MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00149B-LymphocyteHG00149MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00125B-LymphocyteHG00125FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00232B-LymphocyteHG00232FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00174B-LymphocyteHG00174FemaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00122B-LymphocyteHG00122FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00182B-LymphocyteHG00182MaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00110B-LymphocyteHG00110FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00154B-LymphocyteHG00154FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00136B-LymphocyteHG00136MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00251B-LymphocyteHG00251MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00111B-LymphocyteHG00111FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00233B-LymphocyteHG00233FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00189B-LymphocyteHG00189MaleFinnish from Finland (1000 Genomes code: FIN)Not reported
    HG00106B-LymphocyteHG00106FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00252B-LymphocyteHG00252MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00131B-LymphocyteHG00131MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00108B-LymphocyteHG00108MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00119B-LymphocyteHG00119MaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    HG00239B-LymphocyteHG00239FemaleBritish from England and Scotland, UK (1000 Genomes codes: GBR)Not reported
    Sampleset ID:
    3
    Name:
    Follow-up samples (PCR and qPCR)
    Description:
    Samples used for PCR and qPCR follow-up of variants identified in the initial samples. These samples are from the Human Genome Diversity Project (HDGP) collection.
    Size:
    952
    Organisms:
    Homo sapiens
    Sampleset Phenotype(s):
    None reported
  • Download Samples as CSV file
  • Samples for sampleset 3 (displaying 100 of the 952 samples)
    Sample IDSubject ID SexEthnicitySubject Phenotype
    HGDP00080HGDP00080MaleBalochiNot reported
    HGDP00074HGDP00074MaleBalochiNot reported
    HGDP00108HGDP00108MaleHazaraNot reported
    HGDP00169HGDP00169MaleSindhiNot reported
    HGDP00144HGDP00144MaleMakraniNot reported
    HGDP00064HGDP00064MaleBalochiNot reported
    HGDP00146HGDP00146MaleMakraniNot reported
    HGDP00099HGDP00099MaleHazaraNot reported
    HGDP00160HGDP00160MaleMakraniNot reported
    HGDP00157HGDP00157FemaleMakraniNot reported
    HGDP00027HGDP00027MaleBrahuiNot reported
    HGDP00031HGDP00031MaleBrahuiNot reported
    HGDP00092HGDP00092MaleBalochiNot reported
    HGDP00019HGDP00019MaleBrahuiNot reported
    HGDP00124HGDP00124MaleHazaraNot reported
    HGDP00021HGDP00021MaleBrahuiNot reported
    HGDP00158HGDP00158MaleMakraniNot reported
    HGDP00135HGDP00135MaleMakraniNot reported
    HGDP00125HGDP00125MaleHazaraNot reported
    HGDP00005HGDP00005MaleBrahuiNot reported
    HGDP00054HGDP00054MaleBalochiNot reported
    HGDP00049HGDP00049MaleBrahuiNot reported
    HGDP00116HGDP00116MaleHazaraNot reported
    HGDP00052HGDP00052MaleBalochiNot reported
    HGDP00167HGDP00167MaleSindhiNot reported
    HGDP00131HGDP00131MaleMakraniNot reported
    HGDP00119HGDP00119MaleHazaraNot reported
    HGDP00082HGDP00082MaleBalochiNot reported
    HGDP00161HGDP00161MaleMakraniNot reported
    HGDP00029HGDP00029MaleBrahuiNot reported
    HGDP00127HGDP00127MaleHazaraNot reported
    HGDP00009HGDP00009MaleBrahuiNot reported
    HGDP00110HGDP00110MaleHazaraNot reported
    HGDP00045HGDP00045MaleBrahuiNot reported
    HGDP00106HGDP00106MaleHazaraNot reported
    HGDP00122HGDP00122MaleHazaraNot reported
    HGDP00150HGDP00150MaleMakraniNot reported
    HGDP00121HGDP00121MaleHazaraNot reported
    HGDP00115HGDP00115MaleHazaraNot reported
    HGDP00118HGDP00118MaleHazaraNot reported
    HGDP00070HGDP00070MaleBalochiNot reported
    HGDP00139HGDP00139MaleMakraniNot reported
    HGDP00041HGDP00041MaleBrahuiNot reported
    HGDP00151HGDP00151FemaleMakraniNot reported
    HGDP00011HGDP00011MaleBrahuiNot reported
    HGDP00086HGDP00086MaleBalochiNot reported
    HGDP00102HGDP00102MaleHazaraNot reported
    HGDP00003HGDP00003MaleBrahuiNot reported
    HGDP00163HGDP00163MaleSindhiNot reported
    HGDP00141HGDP00141MaleMakraniNot reported
    HGDP00076HGDP00076MaleBalochiNot reported
    HGDP00154HGDP00154FemaleMakraniNot reported
    HGDP00148HGDP00148MaleMakraniNot reported
    HGDP00047HGDP00047MaleBrahuiNot reported
    HGDP00001HGDP00001MaleBrahuiNot reported
    HGDP00165HGDP00165MaleSindhiNot reported
    HGDP00134HGDP00134MaleMakraniNot reported
    HGDP00133HGDP00133MaleMakraniNot reported
    HGDP00155HGDP00155FemaleMakraniNot reported
    HGDP00025HGDP00025MaleBrahuiNot reported
    HGDP00120HGDP00120MaleHazaraNot reported
    HGDP00090HGDP00090MaleBalochiNot reported
    HGDP00058HGDP00058MaleBalochiNot reported
    HGDP00066HGDP00066MaleBalochiNot reported
    HGDP00137HGDP00137MaleMakraniNot reported
    HGDP00105HGDP00105MaleHazaraNot reported
    HGDP00057HGDP00057MaleBalochiNot reported
    HGDP00094HGDP00094MaleBalochiNot reported
    HGDP00068HGDP00068MaleBalochiNot reported
    HGDP00129HGDP00129MaleHazaraNot reported
    HGDP00007HGDP00007MaleBrahuiNot reported
    HGDP00098HGDP00098MaleBalochiNot reported
    HGDP00109HGDP00109MaleHazaraNot reported
    HGDP00078HGDP00078MaleBalochiNot reported
    HGDP00039HGDP00039MaleBrahuiNot reported
    HGDP00143HGDP00143MaleMakraniNot reported
    HGDP00130HGDP00130MaleMakraniNot reported
    HGDP00140HGDP00140MaleMakraniNot reported
    HGDP00023HGDP00023MaleBrahuiNot reported
    HGDP00062HGDP00062MaleBalochiNot reported
    HGDP00056HGDP00056MaleBalochiNot reported
    HGDP00100HGDP00100MaleHazaraNot reported
    HGDP00136HGDP00136MaleMakraniNot reported
    HGDP00088HGDP00088MaleBalochiNot reported
    HGDP00033HGDP00033MaleBrahuiNot reported
    HGDP00017HGDP00017MaleBrahuiNot reported
    HGDP00096HGDP00096MaleBalochiNot reported
    HGDP00035HGDP00035MaleBrahuiNot reported
    HGDP00060HGDP00060MaleBalochiNot reported
    HGDP00149HGDP00149MaleMakraniNot reported
    HGDP00112HGDP00112MaleHazaraNot reported
    HGDP00103HGDP00103MaleHazaraNot reported
    HGDP00104HGDP00104MaleHazaraNot reported
    HGDP00072HGDP00072MaleBalochiNot reported
    HGDP00037HGDP00037MaleBrahuiNot reported
    HGDP00153HGDP00153FemaleMakraniNot reported
    HGDP00013HGDP00013MaleBrahuiNot reported
    HGDP00145HGDP00145MaleMakraniNot reported
    HGDP00015HGDP00015MaleBrahuiNot reported
    HGDP00043HGDP00043MaleBrahuiNot reported

    Experimental Details

    Experiment IDTypeMethodAnalysisPlatformsDataNumber of Variant Calls
    1DiscoveryOligo aCGHProbe signal intensityAgilent Eichler Human CNP 180K v2.1, Agilent Eichler Human CNP 180K v3.0GEO227,380

    Validations

    No validation data were submitted for this study.

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