A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3523n54



Internal ID18995699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19734966..19808815hg38UCSC Ensembl
chr14:20203125..20276974hg19UCSC Ensembl
chr14:19272965..19346814hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3873850
hg1973850
hg1873850
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563767, nsv563768
Samples
Known GenesOR4M1, OR4Q3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3523n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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