A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525033



Internal ID15452326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25707365..25750332hg38UCSC Ensembl
Innerchr20:25688001..25730968hg19UCSC Ensembl
Innerchr20:25636001..25678968hg18UCSC Ensembl
Innerchr20:25636001..25678968hg17UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3842968
hg1942968
hg1842968
hg1742968
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701075
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525033
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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