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nsv9477

  • Variant Calls:13
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:38,765

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 438 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):89,569,883-89,608,647Question Mark
Overlapping variant regions from other studies: 438 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):89,636,291-89,675,055Question Mark
Submitted genomic88,163,792-88,202,556Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv9477RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1689,569,88389,608,647
nsv9477RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1689,636,29189,675,055
nsv9477Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000016.8Chr1688,163,79288,202,556

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv25268copy number gainNA12155Oligo aCGHProbe signal intensity667
nssv28131copy number gainNA19221Oligo aCGHProbe signal intensity857
nssv24149copy number gainNA12740Oligo aCGHProbe signal intensity572
nssv23837copy number gainNA18980Oligo aCGHProbe signal intensity561
nssv26625copy number gainNA19132Oligo aCGHProbe signal intensity684
nssv26791copy number gainNA18502Oligo aCGHProbe signal intensity703
nssv22072copy number lossNA18942Oligo aCGHProbe signal intensity504
nssv22685copy number gainNA10863Oligo aCGHProbe signal intensity530
nssv22770copy number gainNA07029Oligo aCGHProbe signal intensity544
nssv23285copy number gainNA07048Oligo aCGHProbe signal intensity564
nssv24175copy number gainNA12740Oligo aCGHProbe signal intensity572
nssv25927copy number gainNA18504Oligo aCGHProbe signal intensity700
nssv26749copy number gainNA18517Oligo aCGHProbe signal intensity698

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv25268RemappedPerfectNC_000016.10:g.(89
569883_89570567)_(
89604827_89608647)
dup
GRCh38.p12First PassNC_000016.10Chr1689,569,88389,570,56789,604,82789,608,647
nssv28131RemappedPerfectNC_000016.10:g.(89
572391_89573333)_(
89586703_89587552)
dup
GRCh38.p12First PassNC_000016.10Chr1689,572,39189,573,33389,586,70389,587,552
nssv24149RemappedPerfectNC_000016.10:g.(89
573333_89574453)_(
89575054_89577040)
dup
GRCh38.p12First PassNC_000016.10Chr1689,573,33389,574,45389,575,05489,577,040
nssv23837RemappedPerfectNC_000016.10:g.(89
578885_89579443)_(
89580196_89581482)
dup
GRCh38.p12First PassNC_000016.10Chr1689,578,88589,579,44389,580,19689,581,482
nssv26625RemappedPerfectNC_000016.10:g.(89
578885_89579443)_(
89580196_89581482)
dup
GRCh38.p12First PassNC_000016.10Chr1689,578,88589,579,44389,580,19689,581,482
nssv26791RemappedPerfectNC_000016.10:g.(89
578885_89579443)_(
89580196_89581482)
dup
GRCh38.p12First PassNC_000016.10Chr1689,578,88589,579,44389,580,19689,581,482
nssv22072RemappedPerfectNC_000016.10:g.(89
586703_89587552)_(
89588264_89589344)
del
GRCh38.p12First PassNC_000016.10Chr1689,586,70389,587,55289,588,26489,589,344
nssv22685RemappedPerfectNC_000016.10:g.(89
586703_89587552)_(
89588264_89589344)
dup
GRCh38.p12First PassNC_000016.10Chr1689,586,70389,587,55289,588,26489,589,344
nssv22770RemappedPerfectNC_000016.10:g.(89
586703_89587552)_(
89588264_89589344)
dup
GRCh38.p12First PassNC_000016.10Chr1689,586,70389,587,55289,588,26489,589,344
nssv23285RemappedPerfectNC_000016.10:g.(89
586703_89587552)_(
89588264_89589344)
dup
GRCh38.p12First PassNC_000016.10Chr1689,586,70389,587,55289,588,26489,589,344
nssv24175RemappedPerfectNC_000016.10:g.(89
586703_89587552)_(
89588264_89589344)
dup
GRCh38.p12First PassNC_000016.10Chr1689,586,70389,587,55289,588,26489,589,344
nssv25927RemappedPerfectNC_000016.10:g.(89
586703_89587552)_(
89588264_89589344)
dup
GRCh38.p12First PassNC_000016.10Chr1689,586,70389,587,55289,588,26489,589,344
nssv26749RemappedPerfectNC_000016.10:g.(89
586703_89587552)_(
89588264_89589344)
dup
GRCh38.p12First PassNC_000016.10Chr1689,586,70389,587,55289,588,26489,589,344
nssv25268RemappedPerfectNC_000016.9:g.(896
36291_89636975)_(8
9671235_89675055)d
up
GRCh37.p13First PassNC_000016.9Chr1689,636,29189,636,97589,671,23589,675,055
nssv28131RemappedPerfectNC_000016.9:g.(896
38799_89639741)_(8
9653111_89653960)d
up
GRCh37.p13First PassNC_000016.9Chr1689,638,79989,639,74189,653,11189,653,960
nssv24149RemappedPerfectNC_000016.9:g.(896
39741_89640861)_(8
9641462_89643448)d
up
GRCh37.p13First PassNC_000016.9Chr1689,639,74189,640,86189,641,46289,643,448
nssv23837RemappedPerfectNC_000016.9:g.(896
45293_89645851)_(8
9646604_89647890)d
up
GRCh37.p13First PassNC_000016.9Chr1689,645,29389,645,85189,646,60489,647,890
nssv26625RemappedPerfectNC_000016.9:g.(896
45293_89645851)_(8
9646604_89647890)d
up
GRCh37.p13First PassNC_000016.9Chr1689,645,29389,645,85189,646,60489,647,890
nssv26791RemappedPerfectNC_000016.9:g.(896
45293_89645851)_(8
9646604_89647890)d
up
GRCh37.p13First PassNC_000016.9Chr1689,645,29389,645,85189,646,60489,647,890
nssv22072RemappedPerfectNC_000016.9:g.(896
53111_89653960)_(8
9654672_89655752)d
el
GRCh37.p13First PassNC_000016.9Chr1689,653,11189,653,96089,654,67289,655,752
nssv22685RemappedPerfectNC_000016.9:g.(896
53111_89653960)_(8
9654672_89655752)d
up
GRCh37.p13First PassNC_000016.9Chr1689,653,11189,653,96089,654,67289,655,752
nssv22770RemappedPerfectNC_000016.9:g.(896
53111_89653960)_(8
9654672_89655752)d
up
GRCh37.p13First PassNC_000016.9Chr1689,653,11189,653,96089,654,67289,655,752
nssv23285RemappedPerfectNC_000016.9:g.(896
53111_89653960)_(8
9654672_89655752)d
up
GRCh37.p13First PassNC_000016.9Chr1689,653,11189,653,96089,654,67289,655,752
nssv24175RemappedPerfectNC_000016.9:g.(896
53111_89653960)_(8
9654672_89655752)d
up
GRCh37.p13First PassNC_000016.9Chr1689,653,11189,653,96089,654,67289,655,752
nssv25927RemappedPerfectNC_000016.9:g.(896
53111_89653960)_(8
9654672_89655752)d
up
GRCh37.p13First PassNC_000016.9Chr1689,653,11189,653,96089,654,67289,655,752
nssv26749RemappedPerfectNC_000016.9:g.(896
53111_89653960)_(8
9654672_89655752)d
up
GRCh37.p13First PassNC_000016.9Chr1689,653,11189,653,96089,654,67289,655,752
nssv25268Submitted genomicNC_000016.8:g.(881
63792_88164476)_(8
8198736_88202556)d
up
NCBI35 (hg17)NC_000016.8Chr1688,163,79288,164,47688,198,73688,202,556
nssv28131Submitted genomicNC_000016.8:g.(881
66300_88167242)_(8
8180612_88181461)d
up
NCBI35 (hg17)NC_000016.8Chr1688,166,30088,167,24288,180,61288,181,461
nssv24149Submitted genomicNC_000016.8:g.(881
67242_88168362)_(8
8168963_88170949)d
up
NCBI35 (hg17)NC_000016.8Chr1688,167,24288,168,36288,168,96388,170,949
nssv23837Submitted genomicNC_000016.8:g.(881
72794_88173352)_(8
8174105_88175391)d
up
NCBI35 (hg17)NC_000016.8Chr1688,172,79488,173,35288,174,10588,175,391
nssv26625Submitted genomicNC_000016.8:g.(881
72794_88173352)_(8
8174105_88175391)d
up
NCBI35 (hg17)NC_000016.8Chr1688,172,79488,173,35288,174,10588,175,391
nssv26791Submitted genomicNC_000016.8:g.(881
72794_88173352)_(8
8174105_88175391)d
up
NCBI35 (hg17)NC_000016.8Chr1688,172,79488,173,35288,174,10588,175,391
nssv22072Submitted genomicNC_000016.8:g.(881
80612_88181461)_(8
8182173_88183253)d
el
NCBI35 (hg17)NC_000016.8Chr1688,180,61288,181,46188,182,17388,183,253
nssv22685Submitted genomicNC_000016.8:g.(881
80612_88181461)_(8
8182173_88183253)d
up
NCBI35 (hg17)NC_000016.8Chr1688,180,61288,181,46188,182,17388,183,253
nssv22770Submitted genomicNC_000016.8:g.(881
80612_88181461)_(8
8182173_88183253)d
up
NCBI35 (hg17)NC_000016.8Chr1688,180,61288,181,46188,182,17388,183,253
nssv23285Submitted genomicNC_000016.8:g.(881
80612_88181461)_(8
8182173_88183253)d
up
NCBI35 (hg17)NC_000016.8Chr1688,180,61288,181,46188,182,17388,183,253
nssv24175Submitted genomicNC_000016.8:g.(881
80612_88181461)_(8
8182173_88183253)d
up
NCBI35 (hg17)NC_000016.8Chr1688,180,61288,181,46188,182,17388,183,253
nssv25927Submitted genomicNC_000016.8:g.(881
80612_88181461)_(8
8182173_88183253)d
up
NCBI35 (hg17)NC_000016.8Chr1688,180,61288,181,46188,182,17388,183,253
nssv26749Submitted genomicNC_000016.8:g.(881
80612_88181461)_(8
8182173_88183253)d
up
NCBI35 (hg17)NC_000016.8Chr1688,180,61288,181,46188,182,17388,183,253

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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