A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv995n71



Internal ID6318615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2146737..2238288hg19UCSC Ensembl
chr11:2103313..2194864hg18UCSC 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 Variantsnsv896782, nsv896783, nsv896781, nsv896786, nsv896778, nsv896779
SamplesIS37646, IS38176, SP54988, IS41634, IS31045, IS31656, MS11306
Known GenesIGF2, IGF2AS, INS, INS-IGF2, MIR4686, MIR483, TH
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv995n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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