A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3570228



Internal ID18351740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:80080194..80097321hg38UCSC Ensembl
Innerchr5:79376017..79393144hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3817128
hg1917128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9775446
Samples400109LJ
Known GenesTHBS4
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)esv3570228
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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