A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9811211



Internal ID18336002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69990674..70238473hg38UCSC Ensembl
Innerchr16:70024577..70272376hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38247800
hg19247800
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3571442
Supporting Variants
Samples401674DD
Known GenesCLEC18C, LOC100506060, MIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodSNP array
AnalysisWe used four separate algorithms to detect CNVs; Affymetrix Chromosome Analysis Suite (ChAS), iPattern, Nexus and Partek. Our primary analysis was performed based on ChAS CNV calls, which were then supported using the remaining three algorithms to construct a confidence set of CNVs. For all algorithms, we have used 8 probes and >1kb as a base line cutoff for CNV detection.
PlatformAffymetrix CytoScan HD 2.7M array
CommentsNumber of probes=31
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9811211
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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