A curated catalogue of human genomic structural variation

Variant Details

Variant: dgv873e212

Internal ID20149329
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89734780..89738373hg38UCSC Ensembl
chr16:89801188..89804781hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3582440, esv3582446
Samples401165SB, 401912HD, 401812HG, 400507VD, 401474CE, 400532MH, 401858TP, 401117NA, 400270BD, 400739SS, 400325BE, 400671PP, 400150SS, 400880TM, 400626FC, 400645KM, 400084DM, 400425SL, 401997HB, 401852SK
Known GenesFANCA, ZNF276
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
Pubmed ID25503493
Accession Number(s)dgv873e212
Sample Size873
Observed Gain0
Observed Loss20
Observed Complex0

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