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nsv4436486

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:7,150,767
  • Description:chr1:17555508-24706269 complex variant AND Ductal breast carcinoma

Genome View

Select assembly:
Overlapping variant regions from other studies: 20354 SVs from 119 studies. See in: genome view    
Remapped(Score: Perfect):17,229,013-24,379,779Question Mark
Overlapping variant regions from other studies: 20356 SVs from 119 studies. See in: genome view    
Submitted genomic17,555,508-24,706,269Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4436486RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr117,229,01324,379,779
nsv4436486Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr117,555,50824,706,269

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754774complex substitutionMultipleMultipleDuctal breast carcinomaUncertain significanceClinVarRCV000207266.1, VCV000221359.1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv15754774RemappedPerfectGRCh38.p12First PassNC_000001.11Chr117,229,01324,379,779
nssv15754774Submitted genomicGRCh37 (hg19)NC_000001.10Chr117,555,50824,706,269

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv15754774complex substitutionsomaticDuctal breast carcinomaUncertain significanceClinVarRCV000207266.1, VCV000221359.1

No genotype data were submitted for this variant

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