A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983836



Internal ID12629344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19734966..20056096hg38UCSC Ensembl
Innerchr14:20203125..20524255hg19UCSC Ensembl
Innerchr14:19272965..19594095hg18UCSC Ensembl
Innerchr14:19272965..19594095hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38321131
hg19321131
hg18321131
hg17321131
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751264
Supporting Variants
SamplesBEC_633
Known GenesOR4K1, OR4K13, OR4K14, OR4K15, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983836
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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