A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980190



Internal ID12981424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19734966..19918379hg38UCSC Ensembl
Innerchr14:20203125..20386538hg19UCSC Ensembl
Innerchr14:19272965..19456378hg18UCSC Ensembl
Innerchr14:19272965..19456378hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38183414
hg19183414
hg18183414
hg17183414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34555
Supporting Variants
SamplesNA18968
Known GenesOR4K2, OR4M1, OR4N2, OR4Q3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980190
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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