A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562626



Internal ID16350035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86782081..86893902hg38UCSC Ensembl
Innerchr13:87434336..87546157hg19UCSC Ensembl
Innerchr13:86232337..86344158hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38111822
hg19111822
hg18111822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816736
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562626
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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