A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525824



Internal ID15106431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:20068221..20071246hg38UCSC Ensembl
Innerchr20:20048865..20051890hg19UCSC Ensembl
Innerchr20:19996865..19999890hg18UCSC Ensembl
Innerchr20:19996865..19999890hg17UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg383026
hg193026
hg183026
hg173026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702013
Samples
Known GenesC20orf26
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525824
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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