U.S. flag

An official website of the United States government

nsv7066342

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:821,378

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2703 SVs from 100 studies. See in: genome view    
    Submitted genomic84,626,965-85,448,342Question Mark
    Overlapping variant regions from other studies: 2749 SVs from 100 studies. See in: genome view    
    Remapped(Score: Perfect):85,170,196-85,991,573Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066342Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1584,626,96585,448,342
    nsv7066342RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1585,170,19685,991,573

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755207inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755207Submitted genomicNC_000015.10:g.846
    26965_85448342inv
    GRCh38 (hg38)NC_000015.10Chr1584,626,96585,448,342
    nssv18755207RemappedPerfectNC_000015.9:g.8517
    0196_85991573inv
    GRCh37.p13First PassNC_000015.9Chr1585,170,19685,991,573

    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)
    nssv187552074e-061276268
    Support Center