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nsv4455772

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:390,471
  • Description:GRCh37/hg19 11q13.2(chr11:67081259-67471729)x3 AND not provided

Genome View

Select assembly:
Overlapping variant regions from other studies: 1273 SVs from 84 studies. See in: genome view    
Remapped(Score: Perfect):67,313,788-67,704,258Question Mark
Overlapping variant regions from other studies: 1273 SVs from 84 studies. See in: genome view    
Submitted genomic67,081,259-67,471,729Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4455772RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1167,313,78867,704,258
nsv4455772Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1167,081,25967,471,729

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15775677copy number gainMultipleMultiplenot providedUncertain significanceClinVarRCV000847752.2, VCV000687044.23

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15775677RemappedPerfectNC_000011.10:g.(?_
67313788)_(6770425
8_?)dup
GRCh38.p12First PassNC_000011.10Chr1167,313,78867,704,258
nssv15775677Submitted genomicNC_000011.9:g.(?_6
7081259)_(67471729
_?)dup
GRCh37 (hg19)NC_000011.9Chr1167,081,25967,471,729

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15775677GRCh37: NC_000011.9:g.(?_67081259)_(67471729_?)dupcopy number gainunknownnot providedUncertain significanceClinVarRCV000847752.2, VCV000687044.23

No genotype data were submitted for this variant

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