A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520296



Internal ID15447589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:32378142..32378957hg38UCSC Ensembl
Innerchr22:32774129..32774944hg19UCSC Ensembl
Innerchr22:31104129..31104944hg18UCSC Ensembl
Innerchr22:31098683..31099498hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38816
hg19816
hg18816
hg17816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697333
Samples
Known GenesLOC339666
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520296
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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