A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986568



Internal ID12981645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19734966..19951992hg38UCSC Ensembl
Innerchr14:20203125..20420151hg19UCSC Ensembl
Innerchr14:19272965..19489991hg18UCSC Ensembl
Innerchr14:19272965..19489991hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38217027
hg19217027
hg18217027
hg17217027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751204
Supporting Variants
SamplesNA18990
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986568
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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