U.S. flag

An official website of the United States government

nsv7059445

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,498

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 139 SVs from 31 studies. See in: genome view    
    Submitted genomic41,890,316-41,895,813Question Mark
    Overlapping variant regions from other studies: 139 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):42,182,514-42,188,011Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059445Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1541,890,31641,895,813
    nsv7059445RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1542,182,51442,188,011

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754766inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754766Submitted genomicNC_000015.10:g.418
    90316_41895813inv
    GRCh38 (hg38)NC_000015.10Chr1541,890,31641,895,813
    nssv18754766RemappedPerfectNC_000015.9:g.4218
    2514_42188011inv
    GRCh37.p13First PassNC_000015.9Chr1542,182,51442,188,011

    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)
    nssv187547667e-062274758
    Support Center