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nsv4436324

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:8,725,843
  • Description:chr12:10074776-18800953 complex variant AND Ductal breast carcinoma

Genome View

Select assembly:
Overlapping variant regions from other studies: 24511 SVs from 134 studies. See in: genome view    
Remapped(Score: Good):9,922,177-18,648,019Question Mark
Overlapping variant regions from other studies: 24556 SVs from 134 studies. See in: genome view    
Submitted genomic10,074,776-18,800,953Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4436324RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr129,922,17718,648,019
nsv4436324Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1210,074,77618,800,953

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754768complex substitutionMultipleMultipleDuctal breast carcinomaUncertain significanceClinVarRCV000207105.1, VCV000221369.1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv15754768RemappedGoodGRCh38.p12First PassNC_000012.12Chr129,922,17718,648,019
nssv15754768Submitted genomicGRCh37 (hg19)NC_000012.11Chr1210,074,77618,800,953

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754768complex substitutionsomaticDuctal breast carcinomaUncertain significanceClinVarRCV000207105.1, VCV000221369.1

No genotype data were submitted for this variant

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