ChromothripsisDB: a curated database of chromothripsis
 
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  Study
PubMed ID   26833333 Publish Date   2016 Feb
Journal   Am J Hum Genet Species   Homo sapiens
Disease Type   Esophageal Squamous Cell Carcinoma Technology   Next Generation Sequencing
Case Number   1 Raw Data  
Title   Whole-Genome Sequencing Reveals Diverse Models of Structural Variations in Esophageal Squamous Cell Carcinoma
Authors   Cheng C, Zhou Y, Li H, Xiong T, Li S, Bi Y, Kong P, Wang F, Cui H, Li Y, Fang X, Yan T, Li Y, Wang J, Yang B, Zhang L, Jia Z, Song B, Hu X, Yang J, Qiu H, Zhang G, Liu J, Xu E, Shi R, Zhang Y, Liu H, He C, Zhao Z, Qian Y, Rong R, Han Z, Zhang Y, Luo W, Wang J, Peng S, Yang X, Li X, Li L, Fang H, Liu X, Ma L, Chen Y, Guo S, Chen X, Xi Y, Li G, Liang J, Yang X, Guo J, Jia J, Li Q, Cheng X, Zhan Q, Cui Y
Affiliation   Translational Medicine Research Center, Shanxi Medical University, Taiyuan, Shanxi 030001, China; Key Laboratory of Cellular Physiology, Ministry of Education, Shanxi Medical University, Taiyuan, Shanxi 030001, China; Department of Pathology, the First Hospital, Shanxi Medical University, Taiyuan, Shanxi 030001, China
Chromothripsis Definition   Close-by breakpoints: >10
Copy number states: 2
Fragments random joining: Yes
Download   Study Data File
 
Chromothripsis Cases
  ESCC-16T
     
  Case ID: ESCC-16T
  Chromosome:3,8,10
  Disease type: Esophageal Squamous Cell Carcinoma
  Technology: Next Generation Sequencing
  Platform:
  Affected Gene: Gene List
  Download: Copy Number File   Links File
 
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