A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523407



Internal ID15450700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:43842844..43848444hg38UCSC Ensembl
Innerchr20:42471484..42477084hg19UCSC Ensembl
Innerchr20:41904898..41910498hg18UCSC Ensembl
Innerchr20:41904898..41910498hg17UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg385601
hg195601
hg185601
hg175601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699158
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523407
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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