A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523511



Internal ID15104118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:32460579..32637553hg38UCSC Ensembl
Innerchr20:31048382..31225355hg19UCSC Ensembl
Innerchr20:30512043..30689016hg18UCSC Ensembl
Innerchr20:30512043..30689016hg17UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38176975
hg19176974
hg18176974
hg17176974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699283
Samples
Known GenesC20orf112, C20orf203, LOC149950
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523511
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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