A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519733



Internal ID15447026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47825870..47840491hg38UCSC Ensembl
Innerchr22:48221619..48236240hg19UCSC Ensembl
Innerchr22:46600283..46614904hg18UCSC Ensembl
Innerchr22:46542138..46556759hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3814622
hg1914622
hg1814622
hg1714622
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv657995, nssv659202
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519733
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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