A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9816015



Internal ID18348364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:58480806..58484942hg38UCSC Ensembl
Innerchr18:56148038..56152174hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg384137
hg194137
Variant TypeCNV gain
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3574086
Supporting Variants
Samples402042BJ
Known GenesALPK2
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=8
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9816015
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