A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986887



Internal ID12980371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5875654..5933584hg38UCSC Ensembl
Innerchr11:5896884..5954814hg19UCSC Ensembl
Innerchr11:5853460..5911390hg18UCSC Ensembl
Innerchr11:5853460..5911390hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3857931
hg1957931
hg1857931
hg1757931
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34778
Supporting Variants
SamplesNA18571
Known GenesOR52E4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986887
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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