A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv212n21



Internal ID22766404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:22179389..22184462hg38UCSC Ensembl
chr2:22402261..22407334hg19UCSC Ensembl
chr2:22255766..22260839hg18UCSC Ensembl
chr2:22313913..22318986hg17UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg385074
hg195074
hg185074
hg175074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv524414, nsv524885
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv212n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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