A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1193n71



Internal ID6318813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67155210..67294308hg19UCSC Ensembl
chr11:66911786..67050884hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv897805, nsv897813, nsv897809, nsv897806
SamplesSP54988, IS32322, MS16153, IS33504, MS18276
Known GenesAIP, CABP2, CABP4, CARNS1, CDK2AP2, CORO1B, GPR152, LOC100130987, PITPNM1, PPP1CA, PTPRCAP, RAD9A, RPS6KB2, TBC1D10C, TMEM134
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv1193n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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