A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705336



Internal ID15095302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22180477..22180747hg38UCSC Ensembl
Innerchr22:22534867..22535137hg19UCSC Ensembl
Innerchr22:20864867..20865137hg18UCSC Ensembl
Innerchr22:20859421..20859691hg17UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38271
hg19271
hg18271
hg17271
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)nssv705336
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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