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nsv4436605

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:966,076
  • Description:Single allele AND Ductal breast carcinoma

Genome View

Select assembly:
Overlapping variant regions from other studies: 5917 SVs from 105 studies. See in: genome view    
Remapped(Score: Good):870,446-1,836,521Question Mark
Overlapping variant regions from other studies: 5538 SVs from 105 studies. See in: genome view    
Submitted genomic870,446-1,857,751Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4436605RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr11870,4461,836,521
nsv4436605Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr11870,4461,857,751

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754767complex substitutionMultipleMultipleDuctal breast carcinomaUncertain significanceClinVarRCV000207104.1, VCV000221343.1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv15754767RemappedGoodGRCh38.p12First PassNC_000011.10Chr11870,4461,836,521
nssv15754767Submitted genomicGRCh37 (hg19)NC_000011.9Chr11870,4461,857,751

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754767complex substitutionsomaticDuctal breast carcinomaUncertain significanceClinVarRCV000207104.1, VCV000221343.1

No genotype data were submitted for this variant

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