A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6772n71



Internal ID6324392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32583742..32639163hg19UCSC Ensembl
chr6:32691720..32747141hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv885509, nsv885522, nsv885510, nsv885524
SamplesMS18554, IS34599, MS22104, IS41317, MS17130
Known GenesHLA-DQA1, HLA-DQB1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv6772n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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