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nsv7044126

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:211,475

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2104 SVs from 100 studies. See in: genome view    
    Submitted genomic195,494,986-195,706,460Question Mark
    Overlapping variant regions from other studies: 2119 SVs from 100 studies. See in: genome view    
    Remapped(Score: Good):195,221,756-195,433,331Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044126Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3195,494,986195,706,460
    nsv7044126RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3195,221,756195,433,331

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18770954inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18770954Submitted genomicNC_000003.12:g.195
    494986_195706460in
    v
    GRCh38 (hg38)NC_000003.12Chr3195,494,986195,706,460
    nssv18770954RemappedGoodNC_000003.11:g.195
    221756_195433331in
    v
    GRCh37.p13First PassNC_000003.11Chr3195,221,756195,433,331

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv187709547e-062272966
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