A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981119



Internal ID12626149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19798855..19958545hg38UCSC Ensembl
Innerchr14:20267014..20426704hg19UCSC Ensembl
Innerchr14:19336854..19496544hg18UCSC Ensembl
Innerchr14:19336854..19496544hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38159691
hg19159691
hg18159691
hg17159691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751267
Supporting Variants
SamplesBEC_354
Known GenesOR4K1, OR4K2, OR4K5, OR4N2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981119
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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