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nsv901351

  • Variant Calls:15
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:205,927

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2753 SVs from 106 studies. See in: genome view    
Remapped(Score: Perfect):19,750,966-19,956,892Question Mark
Overlapping variant regions from other studies: 2936 SVs from 106 studies. See in: genome view    
Remapped(Score: Perfect):20,219,125-20,425,051Question Mark
Overlapping variant regions from other studies: 1422 SVs from 33 studies. See in: genome view    
Submitted genomic19,288,965-19,494,891Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv901351RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nsv901351RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nsv901351Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1499709copy number gainSP50125SNP arraySNP genotyping analysis18
nssv1521184copy number gainSP52264SNP arraySNP genotyping analysis10
nssv1525585copy number gainSP56724SNP arraySNP genotyping analysis8
nssv1535345copy number gainMS12157SNP arraySNP genotyping analysis13
nssv1537682copy number gainMS13292SNP arraySNP genotyping analysis31
nssv1541896copy number gainMS15528SNP arraySNP genotyping analysis7
nssv1548488copy number gainMS17869SNP arraySNP genotyping analysis15
nssv1551114copy number gainMS18784SNP arraySNP genotyping analysis11
nssv1551946copy number gainMS19023SNP arraySNP genotyping analysis14
nssv1557136copy number gainMS22421SNP arraySNP genotyping analysis17
nssv1559398copy number gainMS23949SNP arraySNP genotyping analysis13
nssv1559752copy number gainMS24108SNP arraySNP genotyping analysis17
nssv1564563copy number gainIS30238SNP arraySNP genotyping analysis16
nssv1571710copy number gainIS32787SNP arraySNP genotyping analysis10
nssv1578159copy number gainIS34698SNP arraySNP genotyping analysis14

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1499709RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1521184RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1525585RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1535345RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1537682RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1541896RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1548488RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1551114RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1551946RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1557136RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1559398RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1559752RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1564563RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1571710RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1578159RemappedPerfectNC_000014.9:g.(197
50966_19755844)_(1
9955706_19956892)d
up
GRCh38.p12First PassNC_000014.9Chr1419,750,96619,755,84419,955,70619,956,892
nssv1499709RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1521184RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1525585RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1535345RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1537682RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1541896RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1548488RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1551114RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1551946RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1557136RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1559398RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1559752RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1564563RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1571710RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1578159RemappedPerfectNC_000014.8:g.(202
19125_20224003)_(2
0423865_20425051)d
up
GRCh37.p13First PassNC_000014.8Chr1420,219,12520,224,00320,423,86520,425,051
nssv1499709Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891
nssv1521184Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891
nssv1525585Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891
nssv1535345Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891
nssv1537682Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891
nssv1541896Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891
nssv1548488Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891
nssv1551114Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891
nssv1551946Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891
nssv1557136Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891
nssv1559398Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891
nssv1559752Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891
nssv1564563Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891
nssv1571710Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891
nssv1578159Submitted genomicNC_000014.7:g.(192
88965_19293843)_(1
9493705_19494891)d
up
NCBI36 (hg18)NC_000014.7Chr1419,288,96519,293,84319,493,70519,494,891

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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