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nsv4436629

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:19,917
  • Description:Single allele AND Ductal breast carcinoma

Genome View

Select assembly:
Overlapping variant regions from other studies: 324 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):21,187,122-21,207,038Question Mark
Overlapping variant regions from other studies: 330 SVs from 56 studies. See in: genome view    
Submitted genomic21,187,121-21,207,037Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4436629RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr921,187,12221,207,038
nsv4436629Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr921,187,12121,207,037

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754719complex substitutionMultipleMultipleDuctal breast carcinomaUncertain significanceClinVarRCV000207325.1, VCV000221342.1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv15754719RemappedPerfectGRCh38.p12First PassNC_000009.12Chr921,187,12221,207,038
nssv15754719Submitted genomicGRCh37 (hg19)NC_000009.11Chr921,187,12121,207,037

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754719complex substitutionsomaticDuctal breast carcinomaUncertain significanceClinVarRCV000207325.1, VCV000221342.1

No genotype data were submitted for this variant

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