A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv173e212



Internal ID22783100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9951359..9981103hg38UCSC Ensembl
chr10:9993322..10023066hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3829745
hg1929745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3578615, esv3578617, esv3578613, esv3578619
Samples400948EV, 400155CW, 400582WS, 400270BD, 401652HL, 400501SJ, 400328LM, 401836SI, 400234CA, 401180GR
Known Genes
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)dgv173e212
Frequency
Sample Size873
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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