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nsv3892460

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:1,681,268
  • Description:GRCh37/hg19 13q12.3-13.1(chr13:32178877-33860144)x0 AND Poly (ADP-Ribose) polymerase inhibitor response

Genome View

Select assembly:
Overlapping variant regions from other studies: 4037 SVs from 104 studies. See in: genome view    
Remapped(Score: Perfect):31,604,740-33,286,007Question Mark
Overlapping variant regions from other studies: 4037 SVs from 104 studies. See in: genome view    
Submitted genomic32,178,877-33,860,144Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv3892460RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1331,604,74033,286,007
nsv3892460Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1332,178,87733,860,144

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15126110copy number lossMultipleMultiplePoly (ADP-Ribose) polymerase inhibitor responsedrug responseClinVarRCV000443876.1, VCV000377385.10

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15126110RemappedPerfectNC_000013.11:g.316
04740_33286007del
GRCh38.p12First PassNC_000013.11Chr1331,604,74033,286,007
nssv15126110Submitted genomicNC_000013.10:g.321
78877_33860144del
GRCh37 (hg19)NC_000013.10Chr1332,178,87733,860,144

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15126110GRCh37: NC_000013.10:g.32178877_33860144delcopy number losssomaticPoly (ADP-Ribose) polymerase inhibitor responsedrug responseClinVarRCV000443876.1, VCV000377385.10

No genotype data were submitted for this variant

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