A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34391



Internal ID12643744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5410754..5472079hg38UCSC Ensembl
Innerchr11:5431984..5493309hg19UCSC Ensembl
Innerchr11:5388560..5449885hg18UCSC Ensembl
Innerchr11:5388560..5449885hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3861326
hg1961326
hg1861326
hg1761326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6980163, essv6980164, essv6987727, essv6989152, essv6980165
SamplesNA18966
Known GenesOR51B5, OR51I1, OR51I2, OR51Q1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34391
Frequency
Sample Size771
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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