A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561909



Internal ID16002632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63419953..64421049hg38UCSC Ensembl
Innerchr13:63994086..64995181hg19UCSC Ensembl
Innerchr13:62892087..63893182hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg381001097
hg191001096
hg181001096
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3192n54
Supporting Variantsnssv812471
Samples
Known GenesLINC00395, OR7E156P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561909
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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