A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980634



Internal ID12982757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55693312..55822820hg38UCSC Ensembl
Innerchr11:55460788..55590296hg19UCSC Ensembl
Innerchr11:55217364..55346872hg18UCSC Ensembl
Innerchr11:55217364..55346872hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38129509
hg19129509
hg18129509
hg17129509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34812
Supporting Variants
SamplesNA19239
Known GenesOR5D13, OR5D14, OR5D18, OR5L1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980634
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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