A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696599



Internal ID15086565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22159186..22162812hg38UCSC Ensembl
Innerchr22:22513579..22517205hg19UCSC Ensembl
Innerchr22:20843579..20847205hg18UCSC Ensembl
Innerchr22:20838133..20841759hg17UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg383627
hg193627
hg183627
hg173627
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)nssv696599
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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