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nsv7073685

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,969,524

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5828 SVs from 102 studies. See in: genome view    
    Submitted genomic72,645,988-74,615,511Question Mark
    Overlapping variant regions from other studies: 5826 SVs from 102 studies. See in: genome view    
    Remapped(Score: Perfect):70,313,223-72,282,747Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073685Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1872,645,98874,615,511
    nsv7073685RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1870,313,22372,282,747

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759526inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759526Submitted genomicNC_000018.10:g.726
    45988_74615511inv
    GRCh38 (hg38)NC_000018.10Chr1872,645,98874,615,511
    nssv18759526RemappedPerfectNC_000018.9:g.7031
    3223_72282747inv
    GRCh37.p13First PassNC_000018.9Chr1870,313,22372,282,747

    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)
    nssv187595264e-061276268
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