A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv785e212



Internal ID19007993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6982157..6989597hg38UCSC Ensembl
chr16:7032158..7039598hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg387441
hg197441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3581977, esv3581965
Samples401962BK, 401563TK, 401278DM, 401589HP, 400606HW
Known GenesRBFOX1
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)dgv785e212
Frequency
Sample Size873
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer