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nsv7073567

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,485,976

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3580 SVs from 91 studies. See in: genome view    
    Submitted genomic73,812,649-75,298,624Question Mark
    Overlapping variant regions from other studies: 3580 SVs from 91 studies. See in: genome view    
    Remapped(Score: Perfect):73,523,694-75,009,668Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073567Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1173,812,64975,298,624
    nsv7073567RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1173,523,69475,009,668

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18734694inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18734694Submitted genomicNC_000011.10:g.738
    12649_75298624inv
    GRCh38 (hg38)NC_000011.10Chr1173,812,64975,298,624
    nssv18734694RemappedPerfectNC_000011.9:g.7352
    3694_75009668inv
    GRCh37.p13First PassNC_000011.9Chr1173,523,69475,009,668

    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)
    nssv187346944e-061276268
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