A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519677



Internal ID15100284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33700149..33702431hg38UCSC Ensembl
Innerchr22:34096135..34098417hg19UCSC Ensembl
Innerchr22:32426135..32428417hg18UCSC Ensembl
Innerchr22:32420689..32422971hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382283
hg192283
hg182283
hg172283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv657537, nssv657744
Samples
Known GenesLARGE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519677
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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