A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2059e212



Internal ID19009267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18994017..19008802hg38UCSC Ensembl
chr8:18851527..18866312hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3814786
hg1914786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3572617, esv3572616, esv3572618, esv3572625, esv3572619
Samples400702PA, 401804FG, 401039PA, 401136LB, 400371GA, 400730SH, 400242TP, 400368SD, 401981GF, 401448BJ, 401056TJ, 401603HH, 401207DA, 401475MK, 400594VJ, 400173KP, 401493HC, 401153HS, 400570RW
Known GenesPSD3
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)dgv2059e212
Frequency
Sample Size873
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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