A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982708



Internal ID12975426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19798855..19945642hg38UCSC Ensembl
Innerchr14:20267014..20413801hg19UCSC Ensembl
Innerchr14:19336854..19483641hg18UCSC Ensembl
Innerchr14:19336854..19483641hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38146788
hg19146788
hg18146788
hg17146788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34980
Supporting Variants
SamplesBEC_581
Known GenesOR4K1, OR4K2, OR4K5, OR4N2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982708
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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