A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3573002



Internal ID18701200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133071168..133079378hg38UCSC Ensembl
Innerchr8:134083413..134091622hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg388211
hg198210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9789916
Samples400574MA
Known GenesSLA, TG
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
Comments
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)esv3573002
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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