A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987812



Internal ID12982627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55693312..55840785hg38UCSC Ensembl
Innerchr11:55460788..55608261hg19UCSC Ensembl
Innerchr11:55217364..55364837hg18UCSC Ensembl
Innerchr11:55217364..55364837hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38147474
hg19147474
hg18147474
hg17147474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35147
Supporting Variants
SamplesNA19209
Known GenesOR5D13, OR5D14, OR5D16, OR5D18, OR5L1, OR5L2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987812
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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