A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613889



Internal ID16054612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25157680..25683222hg38UCSC Ensembl
Innerchr9:25157678..25683220hg19UCSC Ensembl
Innerchr9:25147678..25673220hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38525543
hg19525543
hg18525543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132017
Samples
Known GenesTUSC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613889
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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