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nsv7059534

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,878,669

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 10188 SVs from 109 studies. See in: genome view    
    Submitted genomic51,726,660-55,605,328Question Mark
    Overlapping variant regions from other studies: 10189 SVs from 109 studies. See in: genome view    
    Remapped(Score: Perfect):52,018,857-55,897,526Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059534Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1551,726,66055,605,328
    nsv7059534RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1552,018,85755,897,526

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755725inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755725Submitted genomicNC_000015.10:g.517
    26660_55605328inv
    GRCh38 (hg38)NC_000015.10Chr1551,726,66055,605,328
    nssv18755725RemappedPerfectNC_000015.9:g.5201
    8857_55897526inv
    GRCh37.p13First PassNC_000015.9Chr1552,018,85755,897,526

    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)
    nssv187557252.1e-056274416
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