A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978259



Internal ID12981687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5865016..5947955hg38UCSC Ensembl
Innerchr11:5886246..5969185hg19UCSC Ensembl
Innerchr11:5842822..5925761hg18UCSC Ensembl
Innerchr11:5842822..5925761hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3882940
hg1982940
hg1882940
hg1782940
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34821
Supporting Variants
SamplesNA18994
Known GenesOR52E4, OR56A3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978259
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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