A curated catalogue of human genomic structural variation




Variant Details

Variant: esv35016



Internal ID12991052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98898171..98934460hg38UCSC Ensembl
Innerchr11:98768901..98805190hg19UCSC Ensembl
Innerchr11:98274111..98310400hg18UCSC Ensembl
Innerchr11:98274111..98310400hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3836290
hg1936290
hg1836290
hg1736290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6989065, essv6979089
SamplesNA12891
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv35016
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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