A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv882e212



Internal ID22783809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3585851..3654158hg38UCSC Ensembl
chr17:3489145..3557452hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3868308
hg1968308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3582493, esv3582491, esv3582492
Samples400620MT, 400156WT, 400312CR
Known GenesCTNS, SHPK, TRPV1
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)dgv882e212
Frequency
Sample Size873
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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