A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8089n54



Internal ID20141513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33384911..33386721hg38UCSC Ensembl
chr22:33780897..33782707hg19UCSC Ensembl
chr22:32110897..32112707hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381811
hg191811
hg181811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv588920, nsv588927, nsv588922, nsv588923, nsv588924, nsv588926, nsv588921
Samples
Known GenesLARGE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8089n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss47
Observed Complex0
Frequencyn/a


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