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nsv7065735

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,887

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 794 SVs from 75 studies. See in: genome view    
    Submitted genomic24,853,009-24,873,895Question Mark
    Overlapping variant regions from other studies: 794 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):25,098,156-25,119,042Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065735Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1524,853,00924,873,895
    nsv7065735RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1525,098,15625,119,042

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755930inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755930Submitted genomicNC_000015.10:g.248
    53009_24873895inv
    GRCh38 (hg38)NC_000015.10Chr1524,853,00924,873,895
    nssv18755930RemappedPerfectNC_000015.9:g.2509
    8156_25119042inv
    GRCh37.p13First PassNC_000015.9Chr1525,098,15625,119,042

    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)
    nssv187559301.4e-054274324
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