A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv122n21



Internal ID22766314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20052901..20126230hg38UCSC Ensembl
chr14:20521060..20594389hg19UCSC Ensembl
chr14:19590900..19664229hg18UCSC Ensembl
chr14:19590900..19664229hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3873330
hg1973330
hg1873330
hg1773330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv520054, nsv524732
Samples
Known GenesOR4K17, OR4L1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv122n21
Frequency
Sample Size2026
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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