A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613014



Internal ID16400423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:417918..621779hg38UCSC Ensembl
Innerchr9:417918..621779hg19UCSC Ensembl
Innerchr9:407918..611779hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38203862
hg19203862
hg18203862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1125977
Samples
Known GenesDOCK8, KANK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613014
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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