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nsv4436207

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:4,545
  • Description:Single allele AND Ductal breast carcinoma

Genome View

Select assembly:
Overlapping variant regions from other studies: 302 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):75,737,127-75,741,671Question Mark
Overlapping variant regions from other studies: 302 SVs from 58 studies. See in: genome view    
Submitted genomic75,786,278-75,790,822Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4436207RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr375,737,12775,741,671
nsv4436207Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr375,786,27875,790,822

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754756complex substitutionMultipleMultipleDuctal breast carcinomaUncertain significanceClinVarRCV000207271.1, VCV000221336.1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv15754756RemappedPerfectGRCh38.p12First PassNC_000003.12Chr375,737,12775,741,671
nssv15754756Submitted genomicGRCh37 (hg19)NC_000003.11Chr375,786,27875,790,822

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754756complex substitutionsomaticDuctal breast carcinomaUncertain significanceClinVarRCV000207271.1, VCV000221336.1

No genotype data were submitted for this variant

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