A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979759



Internal ID12980702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19734966..19964829hg38UCSC Ensembl
Innerchr14:20203125..20432988hg19UCSC Ensembl
Innerchr14:19272965..19502828hg18UCSC Ensembl
Innerchr14:19272965..19502828hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38229864
hg19229864
hg18229864
hg17229864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751241
Supporting Variants
SamplesNA18622
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)essv6979759
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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