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nsv7072235

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,194,589

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6490 SVs from 123 studies. See in: genome view    
    Submitted genomic23,679,022-24,873,610Question Mark
    Overlapping variant regions from other studies: 6493 SVs from 123 studies. See in: genome view    
    Remapped(Score: Perfect):23,924,169-25,118,757Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072235Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1523,679,02224,873,610
    nsv7072235RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1523,924,16925,118,757

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755918inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755918Submitted genomicNC_000015.10:g.236
    79022_24873610inv
    GRCh38 (hg38)NC_000015.10Chr1523,679,02224,873,610
    nssv18755918RemappedPerfectNC_000015.9:g.2392
    4169_25118757inv
    GRCh37.p13First PassNC_000015.9Chr1523,924,16925,118,757

    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)
    nssv187559185.7e-0516274720
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