A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699563



Internal ID15089529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3069244..3072609hg38UCSC Ensembl
Innerchr20:3049890..3053255hg19UCSC Ensembl
Innerchr20:2997890..3001255hg18UCSC Ensembl
Innerchr20:2997890..3001255hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383366
hg193366
hg183366
hg173366
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523746
Supporting Variants
Samples
Known GenesOXT
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699563
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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