A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518687



Internal ID15445980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63107763..63122696hg38UCSC Ensembl
Innerchr20:61739115..61754048hg19UCSC Ensembl
Innerchr20:61209560..61224493hg18UCSC Ensembl
Innerchr20:61209560..61224493hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3814934
hg1914934
hg1814934
hg1714934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694066
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518687
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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