A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519765



Internal ID15447058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37252642..37254804hg38UCSC Ensembl
Innerchr22:37648682..37650844hg19UCSC Ensembl
Innerchr22:35978628..35980790hg18UCSC Ensembl
Innerchr22:35973182..35975344hg17UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg382163
hg192163
hg182163
hg172163
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689979, nssv658386, nssv695555
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519765
Frequency
Sample Size2026
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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