A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv263n21



Internal ID22766455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45859124..45862233hg38UCSC Ensembl
chr22:46255004..46258113hg19UCSC Ensembl
chr22:44633668..44636777hg18UCSC Ensembl
chr22:44575541..44578650hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg383110
hg193110
hg183110
hg173110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv518308, nsv526737
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv263n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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