A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5065n71



Internal ID6322685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50918406..50999182hg19UCSC Ensembl
chr22:49265272..49346048hg18UCSC 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 Variantsnsv914546, nsv914548, nsv914549
SamplesIS33248, IS33455, IS32841, IS34005
Known GenesADM2, C22orf41, KLHDC7B, LMF2, MIOX, NCAPH2, ODF3B, SCO2, TYMP
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv5065n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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