WormBase Tree Display for Variation: WBVar00091098

WBVar00091098 Evidence: Paper_evidence: WBPaper00029073
  Name: Public_name: WBVar00091098
    Other_name: niDf77(IV)
  Sequence_details: SMap: S_parent: Sequence: CHROMOSOME_IV
    Flanking_sequences: TGTAGCCTGTAGTCTTCTTGTAGTCCCAATTTGCAGGTGGCCATTAGTTG CTCCCATTCCTACTATTGTTCATCGTCATCGAATGTGAGTTTTCTATCGC
    Mapping_target: CHROMOSOME_IV
    Type_of_mutation: Deletion
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602
    Laboratory: VC
    Person: WBPerson427
    Detection_method: Oligo Array CGH
    Status: Live: Curator_confirmed: WBPerson4025
  Affects: Gene (22)
    Transcript (22)
    Pseudogene: F49F1.8
      R07C12.2
      K08D10.9
      F49F1.13
      R07C12.4
  Reference: WBPaper00029073
  Remark: Flanking sequences represent the nearest array oligo sequences present in the deletion chromsome on the basis of fluorescence ratio. These should not be considered hard breakpoints in the absence of actual sequence data. Original data available on-line at http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE6294.
    This was suppressed because it overlapped with a corrected genome sequence error feature Feature_evidence: WBsf899407
    This was un-suppressed after examination showed it is not changed by the corrected genome sequence error Curator_confirmed: WBPerson4025
  Method: CGH_allele