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nsv516038

  • Variant Calls:18
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:112,309

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 635 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):55,121,748-55,234,056Question Mark
Overlapping variant regions from other studies: 635 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):56,881,508-56,993,816Question Mark
Overlapping variant regions from other studies: 31 SVs from 8 studies. See in: genome view    
Submitted genomic56,551,514-56,663,822Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv516038RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1055,121,74855,234,056
nsv516038RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1056,881,50856,993,816
nsv516038Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000010.8Chr1056,551,51456,663,822

Variant Call Information

Variant Call IDTypeMethodAnalysisZygosity
nssv676481copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv665859copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv703673copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv701222copy number gainSNP arraySNP genotyping analysis
nssv685192copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv655727copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv659956copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv668002copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv672978copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv676102copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv681072copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv684388copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv684560copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv688987copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv689325copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv693892copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv679792copy number lossSNP arraySNP genotyping analysisHeterozygous
nssv684982copy number lossSNP arraySNP genotyping analysisHeterozygous

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv676481RemappedPerfectNC_000010.11:g.(?_
55121748)_(5521548
9_?)del
GRCh38.p12First PassNC_000010.11Chr1055,121,74855,215,489
nssv665859RemappedPerfectNC_000010.11:g.(?_
55127160)_(5521548
9_?)del
GRCh38.p12First PassNC_000010.11Chr1055,127,16055,215,489
nssv703673RemappedPerfectNC_000010.11:g.(?_
55161079)_(5518747
0_?)del
GRCh38.p12First PassNC_000010.11Chr1055,161,07955,187,470
nssv701222RemappedPerfectNC_000010.11:g.(?_
55167660)_(5517786
6_?)dup
GRCh38.p12First PassNC_000010.11Chr1055,167,66055,177,866
nssv685192RemappedPerfectNC_000010.11:g.(?_
55187470)_(5523405
6_?)del
GRCh38.p12First PassNC_000010.11Chr1055,187,47055,234,056
nssv655727RemappedPerfectNC_000010.11:g.(?_
55204437)_(5523405
6_?)del
GRCh38.p12First PassNC_000010.11Chr1055,204,43755,234,056
nssv659956RemappedPerfectNC_000010.11:g.(?_
55204437)_(5523405
6_?)del
GRCh38.p12First PassNC_000010.11Chr1055,204,43755,234,056
nssv668002RemappedPerfectNC_000010.11:g.(?_
55204437)_(5523405
6_?)del
GRCh38.p12First PassNC_000010.11Chr1055,204,43755,234,056
nssv672978RemappedPerfectNC_000010.11:g.(?_
55204437)_(5523405
6_?)del
GRCh38.p12First PassNC_000010.11Chr1055,204,43755,234,056
nssv676102RemappedPerfectNC_000010.11:g.(?_
55204437)_(5523405
6_?)del
GRCh38.p12First PassNC_000010.11Chr1055,204,43755,234,056
nssv681072RemappedPerfectNC_000010.11:g.(?_
55204437)_(5523405
6_?)del
GRCh38.p12First PassNC_000010.11Chr1055,204,43755,234,056
nssv684388RemappedPerfectNC_000010.11:g.(?_
55204437)_(5523405
6_?)del
GRCh38.p12First PassNC_000010.11Chr1055,204,43755,234,056
nssv684560RemappedPerfectNC_000010.11:g.(?_
55204437)_(5523405
6_?)del
GRCh38.p12First PassNC_000010.11Chr1055,204,43755,234,056
nssv688987RemappedPerfectNC_000010.11:g.(?_
55204437)_(5523405
6_?)del
GRCh38.p12First PassNC_000010.11Chr1055,204,43755,234,056
nssv689325RemappedPerfectNC_000010.11:g.(?_
55204437)_(5523405
6_?)del
GRCh38.p12First PassNC_000010.11Chr1055,204,43755,234,056
nssv693892RemappedPerfectNC_000010.11:g.(?_
55204437)_(5523405
6_?)del
GRCh38.p12First PassNC_000010.11Chr1055,204,43755,234,056
nssv679792RemappedPerfectNC_000010.11:g.(?_
55210251)_(5523405
6_?)del
GRCh38.p12First PassNC_000010.11Chr1055,210,25155,234,056
nssv684982RemappedPerfectNC_000010.11:g.(?_
55210251)_(5523405
6_?)del
GRCh38.p12First PassNC_000010.11Chr1055,210,25155,234,056
nssv676481RemappedPerfectNC_000010.10:g.(?_
56881508)_(5697524
9_?)del
GRCh37.p13First PassNC_000010.10Chr1056,881,50856,975,249
nssv665859RemappedPerfectNC_000010.10:g.(?_
56886920)_(5697524
9_?)del
GRCh37.p13First PassNC_000010.10Chr1056,886,92056,975,249
nssv703673RemappedPerfectNC_000010.10:g.(?_
56920839)_(5694723
0_?)del
GRCh37.p13First PassNC_000010.10Chr1056,920,83956,947,230
nssv701222RemappedPerfectNC_000010.10:g.(?_
56927420)_(5693762
6_?)dup
GRCh37.p13First PassNC_000010.10Chr1056,927,42056,937,626
nssv685192RemappedPerfectNC_000010.10:g.(?_
56947230)_(5699381
6_?)del
GRCh37.p13First PassNC_000010.10Chr1056,947,23056,993,816
nssv655727RemappedPerfectNC_000010.10:g.(?_
56964197)_(5699381
6_?)del
GRCh37.p13First PassNC_000010.10Chr1056,964,19756,993,816
nssv659956RemappedPerfectNC_000010.10:g.(?_
56964197)_(5699381
6_?)del
GRCh37.p13First PassNC_000010.10Chr1056,964,19756,993,816
nssv668002RemappedPerfectNC_000010.10:g.(?_
56964197)_(5699381
6_?)del
GRCh37.p13First PassNC_000010.10Chr1056,964,19756,993,816
nssv672978RemappedPerfectNC_000010.10:g.(?_
56964197)_(5699381
6_?)del
GRCh37.p13First PassNC_000010.10Chr1056,964,19756,993,816
nssv676102RemappedPerfectNC_000010.10:g.(?_
56964197)_(5699381
6_?)del
GRCh37.p13First PassNC_000010.10Chr1056,964,19756,993,816
nssv681072RemappedPerfectNC_000010.10:g.(?_
56964197)_(5699381
6_?)del
GRCh37.p13First PassNC_000010.10Chr1056,964,19756,993,816
nssv684388RemappedPerfectNC_000010.10:g.(?_
56964197)_(5699381
6_?)del
GRCh37.p13First PassNC_000010.10Chr1056,964,19756,993,816
nssv684560RemappedPerfectNC_000010.10:g.(?_
56964197)_(5699381
6_?)del
GRCh37.p13First PassNC_000010.10Chr1056,964,19756,993,816
nssv688987RemappedPerfectNC_000010.10:g.(?_
56964197)_(5699381
6_?)del
GRCh37.p13First PassNC_000010.10Chr1056,964,19756,993,816
nssv689325RemappedPerfectNC_000010.10:g.(?_
56964197)_(5699381
6_?)del
GRCh37.p13First PassNC_000010.10Chr1056,964,19756,993,816
nssv693892RemappedPerfectNC_000010.10:g.(?_
56964197)_(5699381
6_?)del
GRCh37.p13First PassNC_000010.10Chr1056,964,19756,993,816
nssv679792RemappedPerfectNC_000010.10:g.(?_
56970011)_(5699381
6_?)del
GRCh37.p13First PassNC_000010.10Chr1056,970,01156,993,816
nssv684982RemappedPerfectNC_000010.10:g.(?_
56970011)_(5699381
6_?)del
GRCh37.p13First PassNC_000010.10Chr1056,970,01156,993,816
nssv676481Submitted genomicNC_000010.8:g.(?_5
6551514)_(56645255
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,551,51456,645,255
nssv665859Submitted genomicNC_000010.8:g.(?_5
6556926)_(56645255
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,556,92656,645,255
nssv703673Submitted genomicNC_000010.8:g.(?_5
6590845)_(56617236
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,590,84556,617,236
nssv701222Submitted genomicNC_000010.8:g.(?_5
6597426)_(56607632
_?)dup
NCBI35 (hg17)NC_000010.8Chr1056,597,42656,607,632
nssv685192Submitted genomicNC_000010.8:g.(?_5
6617236)_(56663822
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,617,23656,663,822
nssv655727Submitted genomicNC_000010.8:g.(?_5
6634203)_(56663822
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,634,20356,663,822
nssv659956Submitted genomicNC_000010.8:g.(?_5
6634203)_(56663822
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,634,20356,663,822
nssv668002Submitted genomicNC_000010.8:g.(?_5
6634203)_(56663822
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,634,20356,663,822
nssv672978Submitted genomicNC_000010.8:g.(?_5
6634203)_(56663822
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,634,20356,663,822
nssv676102Submitted genomicNC_000010.8:g.(?_5
6634203)_(56663822
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,634,20356,663,822
nssv681072Submitted genomicNC_000010.8:g.(?_5
6634203)_(56663822
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,634,20356,663,822
nssv684388Submitted genomicNC_000010.8:g.(?_5
6634203)_(56663822
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,634,20356,663,822
nssv684560Submitted genomicNC_000010.8:g.(?_5
6634203)_(56663822
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,634,20356,663,822
nssv688987Submitted genomicNC_000010.8:g.(?_5
6634203)_(56663822
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,634,20356,663,822
nssv689325Submitted genomicNC_000010.8:g.(?_5
6634203)_(56663822
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,634,20356,663,822
nssv693892Submitted genomicNC_000010.8:g.(?_5
6634203)_(56663822
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,634,20356,663,822
nssv679792Submitted genomicNC_000010.8:g.(?_5
6640017)_(56663822
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,640,01756,663,822
nssv684982Submitted genomicNC_000010.8:g.(?_5
6640017)_(56663822
_?)del
NCBI35 (hg17)NC_000010.8Chr1056,640,01756,663,822

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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