A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522691



Internal ID15449984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:6149378..6149930hg38UCSC Ensembl
Innerchr20:6130025..6130577hg19UCSC Ensembl
Innerchr20:6078025..6078577hg18UCSC Ensembl
Innerchr20:6078025..6078577hg17UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38553
hg19553
hg18553
hg17553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706101
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522691
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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