A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3570327



Internal ID18698525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:107552097..107567712hg38UCSC Ensembl
Innerchr5:106887798..106903413hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3815616
hg1915616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1636e212
Supporting Variantsessv9775768, essv9775771, essv9775770, essv9775765, essv9775764, essv9775769, essv9775766
Samples401183HP, 400320RN, 400082SD, 401333MM, 401762SD, 400845ML, 402060PD
Known GenesEFNA5
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)esv3570327
Frequency
Sample Size873
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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