A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv293n21



Internal ID20132014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98382257..98598992hg38UCSC Ensembl
chr3:98101101..98317836hg19UCSC Ensembl
chr3:99583791..99800526hg18UCSC Ensembl
chr3:99583791..99800526hg17UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38216736
hg19216736
hg18216736
hg17216736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv520503, nsv528056
Samples
Known GenesCLDND1, CPOX, GPR15, OR5K1, OR5K2, OR5K3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv293n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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