A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979662



Internal ID12980555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19734966..19987148hg38UCSC Ensembl
Innerchr14:20203125..20455307hg19UCSC Ensembl
Innerchr14:19272965..19525147hg18UCSC Ensembl
Innerchr14:19272965..19525147hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38252183
hg19252183
hg18252183
hg17252183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34844
Supporting Variants
SamplesNA18594
Known GenesOR4K1, OR4K15, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979662
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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