A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699296



Internal ID15435948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:32965907..32970916hg38UCSC Ensembl
Innerchr20:31553713..31558722hg19UCSC Ensembl
Innerchr20:31017374..31022383hg18UCSC Ensembl
Innerchr20:31017374..31022383hg17UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg385010
hg195010
hg185010
hg175010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523523
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699296
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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