A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9789897



Internal ID18627556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:128112889..128121931hg38UCSC Ensembl
Innerchr8:129125135..129134177hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg389043
hg199043
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3572990
Supporting Variants
Samples400070PC
Known Genes
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=12
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)essv9789897
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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