A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv994n71



Internal ID6318614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2146737..2213166hg19UCSC Ensembl
chr11:2103313..2169742hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv896777, nsv896780
SamplesIS34304, IS35007
Known GenesIGF2, IGF2AS, INS, INS-IGF2, MIR4686, MIR483, TH
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv994n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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