A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654627



Internal ID15044593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25528477..25598046hg38UCSC Ensembl
Innerchr22:25924444..25994013hg19UCSC Ensembl
Innerchr22:24254444..24324013hg18UCSC Ensembl
Innerchr22:24248998..24318567hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3869570
hg1969570
hg1869570
hg1769570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517205
Supporting Variants
Samples
Known GenesADRBK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654627
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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