A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989152



Internal ID12634695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5419054..5460744hg38UCSC Ensembl
Innerchr11:5440284..5481974hg19UCSC Ensembl
Innerchr11:5396860..5438550hg18UCSC Ensembl
Innerchr11:5396860..5438550hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3841691
hg1941691
hg1841691
hg1741691
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)essv6989152
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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