A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979443



Internal ID12980196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19771320..20042948hg38UCSC Ensembl
Innerchr14:20239479..20511107hg19UCSC Ensembl
Innerchr14:19309319..19580947hg18UCSC Ensembl
Innerchr14:19309319..19580947hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38271629
hg19271629
hg18271629
hg17271629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34243
Supporting Variants
SamplesNA18558
Known GenesOR4K1, OR4K13, OR4K14, OR4K15, OR4K2, OR4K5, OR4M1, OR4N2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979443
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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