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nsv4436266

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:194,251
  • Description:Single allele AND Ductal breast carcinoma

Genome View

Select assembly:
Overlapping variant regions from other studies: 697 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):228,165,950-228,360,200Question Mark
Overlapping variant regions from other studies: 698 SVs from 78 studies. See in: genome view    
Submitted genomic228,353,651-228,547,901Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4436266RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1228,165,950228,360,200
nsv4436266Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1228,353,651228,547,901

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754770complex substitutionMultipleMultipleDuctal breast carcinomaUncertain significanceClinVarRCV000207145.1, VCV000221335.1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv15754770RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1228,165,950228,360,200
nssv15754770Submitted genomicGRCh37 (hg19)NC_000001.10Chr1228,353,651228,547,901

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754770complex substitutionsomaticDuctal breast carcinomaUncertain significanceClinVarRCV000207145.1, VCV000221335.1

No genotype data were submitted for this variant

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