A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663676



Internal ID15400328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:32596479..32658860hg38UCSC Ensembl
Innerchr20:31184281..31246662hg19UCSC Ensembl
Innerchr20:30647942..30710323hg18UCSC Ensembl
Innerchr20:30647942..30710323hg17UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3862382
hg1962382
hg1862382
hg1762382
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516018
Supporting Variants
Samples
Known GenesC20orf203, LOC149950
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663676
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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