A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520289



Internal ID15447582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:46340501..46341462hg38UCSC Ensembl
Innerchr20:44969139..44970100hg19UCSC Ensembl
Innerchr20:44402546..44403507hg18UCSC Ensembl
Innerchr20:44402546..44403507hg17UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38962
hg19962
hg18962
hg17962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662430, nssv686183
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520289
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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