A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979551



Internal ID12980374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5864481..5947955hg38UCSC Ensembl
Innerchr11:5885711..5969185hg19UCSC Ensembl
Innerchr11:5842287..5925761hg18UCSC Ensembl
Innerchr11:5842287..5925761hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3883475
hg1983475
hg1883475
hg1783475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34778
Supporting Variants
SamplesNA18571
Known GenesOR52E4, OR56A3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979551
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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