A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982507



Internal ID12973868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19798901..19958501hg38UCSC Ensembl
Innerchr14:20267060..20426660hg19UCSC Ensembl
Innerchr14:19336900..19496500hg18UCSC Ensembl
Innerchr14:19336900..19496500hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38159601
hg19159601
hg18159601
hg17159601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751221
Supporting Variants
SamplesBEC_460
Known GenesOR4K1, OR4K2, OR4K5, OR4N2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982507
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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