A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5062n71



Internal ID6322682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50837814..51024308hg19UCSC Ensembl
chr22:49184680..49371174hg18UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv914534, nsv914538, nsv914533, nsv914539, nsv914540, nsv914536
SamplesMS10311, MS17208, IS40297, MS16153, IS39233, IS33239
Known GenesADM2, C22orf41, CHKB, CHKB-CPT1B, CPT1B, KLHDC7B, LMF2, LOC100144603, MIOX, NCAPH2, ODF3B, PPP6R2, SBF1, SCO2, TYMP
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv5062n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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