A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3520n54



Internal ID22771415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19698109..19977459hg38UCSC Ensembl
chr14:20166268..20445618hg19UCSC Ensembl
chr14:19236108..19515458hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38279351
hg19279351
hg18279351
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563749, nsv563764, nsv563747, nsv563763, nsv563750, nsv563791, nsv563779, nsv563770, nsv563771, nsv563776, nsv563759, nsv563790, nsv563773, nsv563772, nsv563761, nsv563758, nsv563777, nsv563760, nsv563778, nsv563762, nsv563775
Samples
Known GenesOR11H2, OR4K1, OR4K15, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3520n54
Frequency
Sample Size17421
Observed Gain69
Observed Loss0
Observed Complex0
Frequencyn/a


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