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nsv4436354

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:6,739,807
  • Description:Single allele AND Ductal breast carcinoma

Genome View

Select assembly:
Overlapping variant regions from other studies: 19449 SVs from 132 studies. See in: genome view    
Remapped(Score: Perfect):9,682,848-16,422,654Question Mark
Overlapping variant regions from other studies: 19449 SVs from 132 studies. See in: genome view    
Submitted genomic9,586,165-16,325,968Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4436354RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr179,682,84816,422,654
nsv4436354Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000017.10Chr179,586,16516,325,968

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754769complex substitutionMultipleMultipleDuctal breast carcinomaUncertain significanceClinVarRCV000207129.1, VCV000221346.1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv15754769RemappedPerfectGRCh38.p12First PassNC_000017.11Chr179,682,84816,422,654
nssv15754769Submitted genomicGRCh37 (hg19)NC_000017.10Chr179,586,16516,325,968

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754769complex substitutionsomaticDuctal breast carcinomaUncertain significanceClinVarRCV000207129.1, VCV000221346.1

No genotype data were submitted for this variant

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