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nsv7054407

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,403

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 166 SVs from 27 studies. See in: genome view    
    Submitted genomic186,950,990-186,957,392Question Mark
    Overlapping variant regions from other studies: 166 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):186,920,122-186,926,524Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054407Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1186,950,990186,957,392
    nsv7054407RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1186,920,122186,926,524

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18739105inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18739105Submitted genomicNC_000001.11:g.186
    950990_186957392in
    v
    GRCh38 (hg38)NC_000001.11Chr1186,950,990186,957,392
    nssv18739105RemappedPerfectNC_000001.10:g.186
    920122_186926524in
    v
    GRCh37.p13First PassNC_000001.10Chr1186,920,122186,926,524

    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)
    nssv187391054e-061276216
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