A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980165



Internal ID12634681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5419057..5460743hg38UCSC Ensembl
Innerchr11:5440287..5481973hg19UCSC Ensembl
Innerchr11:5396863..5438549hg18UCSC Ensembl
Innerchr11:5396863..5438549hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3841687
hg1941687
hg1841687
hg1741687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34391
Supporting Variants
SamplesNA18966
Known GenesOR51B5, OR51I1, OR51I2, OR51Q1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980165
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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