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nsv4436633

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:1,978,920
  • Description:chr19:36674305-38652962 complex variant AND Ductal breast carcinoma

Genome View

Select assembly:
Overlapping variant regions from other studies: 6829 SVs from 101 studies. See in: genome view    
Remapped(Score: Good):36,183,403-38,162,322Question Mark
Overlapping variant regions from other studies: 6825 SVs from 101 studies. See in: genome view    
Submitted genomic36,674,305-38,652,962Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4436633RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1936,183,40338,162,322
nsv4436633Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000019.9Chr1936,674,30538,652,962

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754741complex substitutionMultipleMultipleDuctal breast carcinomaUncertain significanceClinVarRCV000207036.1, VCV000221351.1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv15754741RemappedGoodGRCh38.p12First PassNC_000019.10Chr1936,183,40338,162,322
nssv15754741Submitted genomicGRCh37 (hg19)NC_000019.9Chr1936,674,30538,652,962

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754741complex substitutionsomaticDuctal breast carcinomaUncertain significanceClinVarRCV000207036.1, VCV000221351.1

No genotype data were submitted for this variant

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