A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704076



Internal ID15094042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22179189..22180477hg38UCSC Ensembl
Innerchr22:22533579..22534867hg19UCSC Ensembl
Innerchr22:20863579..20864867hg18UCSC Ensembl
Innerchr22:20858133..20859421hg17UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg381289
hg191289
hg181289
hg171289
Variant TypeCNV gain
Copy Number
Allele State
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)nssv704076
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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