A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659051



Internal ID15395703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45727555..45749534hg38UCSC Ensembl
Innerchr20:44356194..44378173hg19UCSC Ensembl
Innerchr20:43789608..43811580hg18UCSC Ensembl
Innerchr20:43789608..43811580hg17UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3821980
hg1921980
hg1821973
hg1721973
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517420
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659051
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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