A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5067n71



Internal ID6322687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50952570..51070285hg19UCSC Ensembl
chr22:49299436..49417151hg18UCSC 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 Variantsnsv914560, nsv914557, nsv914558, nsv914555
SamplesSP54956, IS40502, IS30369, IS35968
Known GenesARSA, C22orf41, CHKB, CHKB-CPT1B, CPT1B, KLHDC7B, LOC100144603, MAPK8IP2, NCAPH2, ODF3B, SCO2, TYMP
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv5067n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer