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nsv6912549

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:153,863

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 623 SVs from 71 studies. See in: genome view    
    Submitted genomic55,917,267-56,071,129Question Mark
    Overlapping variant regions from other studies: 626 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):55,684,743-55,838,605Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6912549Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1155,917,26756,071,129
    nsv6912549RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1155,684,74355,838,605

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351626deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351626Submitted genomicNC_000011.10:g.559
    17267_56071129del
    GRCh38 (hg38)NC_000011.10Chr1155,917,26756,071,129
    nssv18351626RemappedPerfectNC_000011.9:g.5568
    4743_55838605del
    GRCh37.p13First PassNC_000011.9Chr1155,684,74355,838,605

    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)
    nssv183516260.002572273496
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