A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv997n71



Internal ID6318617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2173447..2241272hg19UCSC Ensembl
chr11:2130023..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 Variantsnsv896791, nsv896799, nsv896790, nsv896788, nsv896789, nsv896800
SamplesSP54956, IS41243, IS37172, MS10386, MS17208, MS16315, MS18276, MS10698, MS10769
Known GenesINS, INS-IGF2, MIR4686, TH
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv997n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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