A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524629



Internal ID15451922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:30849758..30858967hg38UCSC Ensembl
Innerchr22:31245745..31254954hg19UCSC Ensembl
Innerchr22:29575745..29584954hg18UCSC Ensembl
Innerchr22:29570299..29579508hg17UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg389210
hg199210
hg189210
hg179210
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700592
Samples
Known GenesOSBP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524629
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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