A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562427



Internal ID16349836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:80109490..80116000hg38UCSC Ensembl
Innerchr13:80683625..80690135hg19UCSC Ensembl
Innerchr13:79581626..79588136hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg386511
hg196511
hg186511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv815961
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562427
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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