A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694053



Internal ID15430705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58729218..58738436hg38UCSC Ensembl
Innerchr20:57304274..57313492hg19UCSC Ensembl
Innerchr20:56737668..56746887hg18UCSC Ensembl
Innerchr20:56737668..56746887hg17UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg389219
hg199219
hg189220
hg179220
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521973
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694053
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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