A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979636



Internal ID12980516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19734966..19909567hg38UCSC Ensembl
Innerchr14:20203125..20377726hg19UCSC Ensembl
Innerchr14:19272965..19447566hg18UCSC Ensembl
Innerchr14:19272965..19447566hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38174602
hg19174602
hg18174602
hg17174602
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751260
Supporting Variants
SamplesNA18592
Known GenesOR4K2, OR4M1, OR4N2, OR4Q3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979636
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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