A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520286



Internal ID15447579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37252642..37261499hg38UCSC Ensembl
Innerchr22:37648682..37657539hg19UCSC Ensembl
Innerchr22:35978628..35987485hg18UCSC Ensembl
Innerchr22:35973182..35982039hg17UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg388858
hg198858
hg188858
hg178858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697326
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520286
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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