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nsv6624961

  • Variant Calls:4
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31,722

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1030 SVs from 87 studies. See in: genome view    
Remapped(Score: Perfect):40,850,020-40,881,741Question Mark
Overlapping variant regions from other studies: 1030 SVs from 87 studies. See in: genome view    
Submitted genomic41,355,925-41,387,646Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv6624961RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1940,850,02040,881,741
nsv6624961Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000019.9Chr1941,355,92541,387,646

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv18301934deletionOSC5865SNP arrayProbe signal intensity10
nssv18303096deletionOSC6020SNP arrayProbe signal intensity9
nssv18308173deletionOSC6766SNP arrayProbe signal intensity10
nssv18319809deletionOSC8831SNP arrayProbe signal intensity15

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv18301934RemappedPerfectNC_000019.10:g.(?_
40850020)_(4088174
1_?)del
GRCh38.p12First PassNC_000019.10Chr1940,850,02040,881,741
nssv18303096RemappedPerfectNC_000019.10:g.(?_
40850020)_(4088174
1_?)del
GRCh38.p12First PassNC_000019.10Chr1940,850,02040,881,741
nssv18308173RemappedPerfectNC_000019.10:g.(?_
40850020)_(4088174
1_?)del
GRCh38.p12First PassNC_000019.10Chr1940,850,02040,881,741
nssv18319809RemappedPerfectNC_000019.10:g.(?_
40850020)_(4088174
1_?)del
GRCh38.p12First PassNC_000019.10Chr1940,850,02040,881,741
nssv18301934Submitted genomicNC_000019.9:g.(?_4
1355925)_(41387646
_?)del
GRCh37 (hg19)NC_000019.9Chr1941,355,92541,387,646
nssv18303096Submitted genomicNC_000019.9:g.(?_4
1355925)_(41387646
_?)del
GRCh37 (hg19)NC_000019.9Chr1941,355,92541,387,646
nssv18308173Submitted genomicNC_000019.9:g.(?_4
1355925)_(41387646
_?)del
GRCh37 (hg19)NC_000019.9Chr1941,355,92541,387,646
nssv18319809Submitted genomicNC_000019.9:g.(?_4
1355925)_(41387646
_?)del
GRCh37 (hg19)NC_000019.9Chr1941,355,92541,387,646

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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