A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1194n71



Internal ID6318814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67155210..67419855hg19UCSC Ensembl
chr11:66911786..67176431hg18UCSC 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 Variantsnsv897807, nsv897808
SamplesIS33684, MS10769
Known GenesACY3, AIP, CABP2, CABP4, CARNS1, CDK2AP2, CORO1B, DOC2GP, GPR152, GSTP1, LOC100130987, NDUFV1, NUDT8, PITPNM1, PPP1CA, PTPRCAP, RAD9A, RPS6KB2, TBC1D10C, TBX10, TMEM134
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv1194n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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