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nsv4387131

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:223,583

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 628 SVs from 69 studies. See in: genome view    
Remapped(Score: Perfect):32,890,166-33,113,748Question Mark
Overlapping variant regions from other studies: 628 SVs from 69 studies. See in: genome view    
Submitted genomic33,355,767-33,579,349Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4387131RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr132,890,16633,113,748
nsv4387131Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr133,355,76733,579,349

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15621560copy number gain1-1005-003SNP arrayGenotyping16

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15621560RemappedPerfectNC_000001.11:g.(?_
32890166)_(3311374
8_?)dup
GRCh38.p12First PassNC_000001.11Chr132,890,16633,113,748
nssv15621560Submitted genomicNC_000001.10:g.(?_
33355767)_(3357934
9_?)dup
GRCh37 (hg19)NC_000001.10Chr133,355,76733,579,349

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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