A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699051



Internal ID15089017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22109835..22110115hg38UCSC Ensembl
Innerchr22:22464245..22464525hg19UCSC Ensembl
Innerchr22:20794245..20794525hg18UCSC Ensembl
Innerchr22:20788799..20789079hg17UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38281
hg19281
hg18281
hg17281
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)nssv699051
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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