A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv170e212



Internal ID22783097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:898556..936659hg38UCSC Ensembl
chr10:944496..982599hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3838104
hg1938104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3578579, esv3578584, esv3578581
Samples401487FW, 401783BD, 400743LS, 400073HT, 400320RN, 400352CA, 401939GD, 401717LP, 400136DM, 400458LS, 401295HB, 401277RA, 400072GR
Known GenesLARP4B
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)dgv170e212
Frequency
Sample Size873
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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