ChromothripsisDB: a curated database of chromothripsis
 
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PubMed ID   29073611 Publish Date   2017 Oct
Journal   Cytogenet Genome Res. Species   Homo sapiens
Disease Type   Recurrent pregnancy loss Technology   Next Generation Sequencing
Case Number   6 Raw Data  
Title   Genomic Characterization of Chromosomal Insertions: Insights into the Mechanisms Underlying Chromothripsis
Authors   Kato T, Ouchi Y, Inagaki H, Makita Y, Mizuno S, Kajita M, Ikeda T, Takeuchi K, Kurahashi H
Affiliation   Division of Molecular Genetics, Institute for Comprehensive Medical Science (ICMS), Fujita Health University, Toyoake, Japan
Chromothripsis Definition   Close-by breakpoints: 6
Copy number states: >=2
Fragments random joining: Yes
Download   Study Data File
 
Chromothripsis Cases
  case_1
     
  Case ID: case_1
  Chromosome:4,14
  Disease type: Developmental delay
  Technology: Next Generation Sequencing
  Platform: Illumina HiSeq 1500
  Download: Copy Number File   
  case_3
     
  Case ID: case_3
  Chromosome:8,10,12
  Disease type: Langer-Giedion syndrome
  Technology: Next Generation Sequencing
  Platform: Illumina HiSeq 1500
  Download: Copy Number File   
  case_4
     
  Case ID: case_4
  Chromosome:7
  Disease type: Recurrent pregnancy loss
  Technology: Next Generation Sequencing
  Platform: Illumina HiSeq 1500
  Download: Copy Number File   
  case_1
     
  Case ID: case_1
  Chromosome:4,14
  Disease type: Developmental delay
  Technology: Next Generation Sequencing
  Platform: Illumina HiSeq 1500
  Download: Copy Number File   
  case_3
     
  Case ID: case_3
  Chromosome:8,10,12
  Disease type: Langer-Giedion syndrome
  Technology: Next Generation Sequencing
  Platform: Illumina HiSeq 1500
  Download: Copy Number File   
  case_4
     
  Case ID: case_4
  Chromosome:7
  Disease type: Recurrent pregnancy loss
  Technology: Next Generation Sequencing
  Platform: Illumina HiSeq 1500
  Download: Copy Number File   
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