U.S. flag

An official website of the United States government

nsv7068553

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,971

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 147 SVs from 38 studies. See in: genome view    
    Submitted genomic45,387,251-45,392,221Question Mark
    Overlapping variant regions from other studies: 147 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):45,890,509-45,895,479Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068553Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1945,387,25145,392,221
    nsv7068553RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1945,890,50945,895,479

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760794inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760794Submitted genomicNC_000019.10:g.453
    87251_45392221inv
    GRCh38 (hg38)NC_000019.10Chr1945,387,25145,392,221
    nssv18760794RemappedPerfectNC_000019.9:g.4589
    0509_45895479inv
    GRCh37.p13First PassNC_000019.9Chr1945,890,50945,895,479

    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)
    nssv187607944e-061276268
    Support Center