A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1069n71



Internal ID6318689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34253683..34621004hg19UCSC Ensembl
chr11:34210259..34577580hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv897208, nsv897207
SamplesIS32843, IS35299
Known GenesABTB2, CAT, ELF5
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv1069n71
Frequency
Sample Size6533
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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