A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979421



Internal ID12980174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19771320..19954424hg38UCSC Ensembl
Innerchr14:20239479..20422583hg19UCSC Ensembl
Innerchr14:19309319..19492423hg18UCSC Ensembl
Innerchr14:19309319..19492423hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38183105
hg19183105
hg18183105
hg17183105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34625
Supporting Variants
SamplesNA18552
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)essv6979421
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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