A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694309



Internal ID15430961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:60043196..60045305hg38UCSC Ensembl
Innerchr20:58618251..58620360hg19UCSC Ensembl
Innerchr20:58051646..58053755hg18UCSC Ensembl
Innerchr20:58051646..58053755hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382110
hg192110
hg182110
hg172110
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519134
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694309
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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