A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613793



Internal ID16401202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23185204..23226245hg38UCSC Ensembl
Innerchr9:23185202..23226243hg19UCSC Ensembl
Innerchr9:23175202..23216243hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3841042
hg1941042
hg1841042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1131407
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613793
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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