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nsv7049138

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:105,720

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 614 SVs from 89 studies. See in: genome view    
    Submitted genomic193,070,073-193,175,792Question Mark
    Overlapping variant regions from other studies: 614 SVs from 89 studies. See in: genome view    
    Remapped(Score: Perfect):192,787,862-192,893,581Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7049138Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3193,070,073193,175,792
    nsv7049138RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3192,787,862192,893,581

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18770921inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18770921Submitted genomicNC_000003.12:g.193
    070073_193175792in
    v
    GRCh38 (hg38)NC_000003.12Chr3193,070,073193,175,792
    nssv18770921RemappedPerfectNC_000003.11:g.192
    787862_192893581in
    v
    GRCh37.p13First PassNC_000003.11Chr3192,787,862192,893,581

    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)
    nssv187709218.9e-0525274414
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