A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613887



Internal ID16401296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25027432..25119901hg38UCSC Ensembl
Innerchr9:25027430..25119899hg19UCSC Ensembl
Innerchr9:25017430..25109899hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3892470
hg1992470
hg1892470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156910
Samples1780854576_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613887
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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