A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984314



Internal ID12630101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19798901..19964901hg38UCSC Ensembl
Innerchr14:20267060..20433060hg19UCSC Ensembl
Innerchr14:19336900..19502900hg18UCSC Ensembl
Innerchr14:19336900..19502900hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38166001
hg19166001
hg18166001
hg17166001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751268
Supporting Variants
SamplesBEC_688
Known GenesOR4K1, OR4K2, OR4K5, OR4N2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984314
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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