A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978412



Internal ID12981942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55677818..55853223hg38UCSC Ensembl
Innerchr11:55445294..55620699hg19UCSC Ensembl
Innerchr11:55201870..55377275hg18UCSC Ensembl
Innerchr11:55201870..55377275hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38175406
hg19175406
hg18175406
hg17175406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35012
Supporting Variants
SamplesNA19094
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)essv6978412
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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