A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702380



Internal ID15092346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25244661..25303640hg38UCSC Ensembl
Innerchr22:25640628..25699607hg19UCSC Ensembl
Innerchr22:23970628..24029607hg18UCSC Ensembl
Innerchr22:23965182..24024161hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3858980
hg1958980
hg1858980
hg1758980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517205
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702380
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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