A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702261



Internal ID15092227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33364618..33380444hg38UCSC Ensembl
Innerchr22:33760604..33776430hg19UCSC Ensembl
Innerchr22:32090604..32106430hg18UCSC Ensembl
Innerchr22:32085158..32100984hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3815827
hg1915827
hg1815827
hg1715827
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526030
Supporting Variants
Samples
Known GenesLARGE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702261
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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