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nsv4436579

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:698,313
  • Description:chr11:1092954..1857751 complex variant AND Ductal breast carcinoma

Genome View

Select assembly:
Overlapping variant regions from other studies: 3998 SVs from 98 studies. See in: genome view    
Remapped(Score: Pass):1,138,209-1,836,521Question Mark
Overlapping variant regions from other studies: 4130 SVs from 99 studies. See in: genome view    
Submitted genomic1,092,954-1,857,751Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4436579RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr111,138,2091,836,521
nsv4436579Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr111,092,9541,857,751

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754773complex substitutionMultipleMultipleDuctal breast carcinomaUncertain significanceClinVarRCV000207239.1, VCV000221367.1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv15754773RemappedPassGRCh38.p12First PassNC_000011.10Chr111,138,2091,836,521
nssv15754773Submitted genomicGRCh37 (hg19)NC_000011.9Chr111,092,9541,857,751

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754773complex substitutionsomaticDuctal breast carcinomaUncertain significanceClinVarRCV000207239.1, VCV000221367.1

No genotype data were submitted for this variant

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