A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528767



Internal ID15456060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37242920..37254804hg38UCSC Ensembl
Innerchr22:37638960..37650844hg19UCSC Ensembl
Innerchr22:35968906..35980790hg18UCSC Ensembl
Innerchr22:35963460..35975344hg17UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3811885
hg1911885
hg1811885
hg1711885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705431
Samples
Known GenesRAC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528767
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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