ChromothripsisDB: a curated database of chromothripsis
 
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PubMed ID   25799107 Publish Date   2015 Apr
Journal   Am J Hum Genet Species   Homo sapiens
Disease Type   Congenital abnormality Technology   Next Generation Sequencing
Case Number   3 Raw Data   GEO: GSE65454  
Title   Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring
Authors   de Pagter MS, van Roosmalen MJ, Baas AF, Renkens I, Duran KJ, van Binsbergen E, Tavakoli-Yaraki M, Hochstenbach R, van der Veken LT, Cuppen E, Kloosterman WP
Affiliation   Department of Medical Genetics, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht 3584 CG, the Netherlands
Chromothripsis Definition   Close-by breakpoints: >=6
Copy number states: 5
Fragments random joining: Yes
Download   Study Data File
 
Chromothripsis Cases
  Mother1
     
  Case ID: Mother1
  Chromosome:9,10,14,16
  Disease type: Congenital abnormality
  Technology: Next Generation Sequencing
  Platform: AB SOLiD 4 System
  Affected Gene: Gene List
  Download: Links File
  Mother2
     
  Case ID: Mother2
  Chromosome:6,7,9,10,12
  Disease type: Congenital abnormality
  Technology: Next Generation Sequencing
  Platform: AB SOLiD 4 System
  Affected Gene: Gene List
  Download: Links File
  Mother3
     
  Case ID: Mother3
  Chromosome:1,3,5
  Disease type: Congenital abnormality
  Technology: Next Generation Sequencing
  Platform: AB SOLiD 4 System
  Affected Gene: Gene List
  Download: Links File
 
© 2015 Cai Laboratory.  Last updated on 13 Mar 2018