A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694868



Internal ID15084834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22074462..22075818hg38UCSC Ensembl
Innerchr22:22428873..22430229hg19UCSC Ensembl
Innerchr22:20758873..20760229hg18UCSC Ensembl
Innerchr22:20753427..20754783hg17UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg381357
hg191357
hg181357
hg171357
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516394
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694868
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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