A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1705e212



Internal ID22784632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:294124..385771hg38UCSC Ensembl
chr6:294124..385771hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3891648
hg1991648
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3576085, esv3576071, esv3576076, esv3576080, esv3576086, esv3576079, esv3575984, esv3576075, esv3576078, esv3576084, esv3576077, esv3576074, esv3576081, esv3576082, esv3576073
Samples400911GA, 401052BM, 401146US, 400083TG, 400655WB, 401824MM, 400855BD, 400509CJ, 401297KC, 400033KC, 400307HW, 401550SP, 400442FE, 401027KW, 402033WD, 401477ST, 401125LM, 400122PL, 401804FG, 401526WB, 401825TH, 400171BJ, 401359HF, 401361GG, 400728PB, 400235MP, 402048WB, 400792RE, 401543DC, 401607LL, 401882CR, 400138LA
Known GenesDUSP22
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)dgv1705e212
Frequency
Sample Size873
Observed Gain32
Observed Loss0
Observed Complex0
Frequencyn/a


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