A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979462



Internal ID12980229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19771087..19964642hg38UCSC Ensembl
Innerchr14:20239246..20432801hg19UCSC Ensembl
Innerchr14:19309086..19502641hg18UCSC Ensembl
Innerchr14:19309086..19502641hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38193556
hg19193556
hg18193556
hg17193556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751238
Supporting Variants
SamplesNA18561
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979462
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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