A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv992n71



Internal ID6318612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2087220..2241272hg19UCSC Ensembl
chr11:2043796..2197848hg18UCSC 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 Variantsnsv896770, nsv896775, nsv896774, nsv896773
SamplesMS10123, MS10311, IS32841, IS39233
Known GenesIGF2, IGF2AS, INS, INS-IGF2, MIR4686, MIR483, TH
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv992n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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