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nsv4436231

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:28,429
  • Description:chr20:61880169-61908597 complex variant AND Ductal breast carcinoma

Genome View

Select assembly:
Overlapping variant regions from other studies: 253 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):63,248,817-63,277,245Question Mark
Overlapping variant regions from other studies: 253 SVs from 57 studies. See in: genome view    
Submitted genomic61,880,169-61,908,597Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4436231RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2063,248,81763,277,245
nsv4436231Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000020.10Chr2061,880,16961,908,597

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754742complex substitutionMultipleMultipleDuctal breast carcinomaUncertain significanceClinVarRCV000207048.1, VCV000221371.1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv15754742RemappedPerfectGRCh38.p12First PassNC_000020.11Chr2063,248,81763,277,245
nssv15754742Submitted genomicGRCh37 (hg19)NC_000020.10Chr2061,880,16961,908,597

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754742complex substitutionsomaticDuctal breast carcinomaUncertain significanceClinVarRCV000207048.1, VCV000221371.1

No genotype data were submitted for this variant

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