A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699081



Internal ID15435733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:40692868..40707609hg38UCSC Ensembl
Innerchr22:41088872..41103613hg19UCSC Ensembl
Innerchr22:39418818..39433559hg18UCSC Ensembl
Innerchr22:39413372..39428113hg17UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3814742
hg1914742
hg1814742
hg1714742
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523335
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699081
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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