A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979444



Internal ID12980197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19798855..19951992hg38UCSC Ensembl
Innerchr14:20267014..20420151hg19UCSC Ensembl
Innerchr14:19336854..19489991hg18UCSC Ensembl
Innerchr14:19336854..19489991hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38153138
hg19153138
hg18153138
hg17153138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34243
Supporting Variants
SamplesNA18558
Known GenesOR4K1, OR4K2, OR4K5, OR4N2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979444
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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