A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987727



Internal ID12634676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5410756..5472079hg38UCSC Ensembl
Innerchr11:5431986..5493309hg19UCSC Ensembl
Innerchr11:5388562..5449885hg18UCSC Ensembl
Innerchr11:5388562..5449885hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3861324
hg1961324
hg1861324
hg1761324
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)essv6987727
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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