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nsv6515868

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:623

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 92 SVs from 20 studies. See in: genome view    
    Submitted genomic55,430,888-55,431,510Question Mark
    Overlapping variant regions from other studies: 91 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):55,942,255-55,942,877Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6515868Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1955,430,88855,431,510
    nsv6515868RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1955,942,25555,942,877

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18049181deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18049181Submitted genomicNC_000019.10:g.554
    30888_55431510del
    GRCh38 (hg38)NC_000019.10Chr1955,430,88855,431,510
    nssv18049181RemappedPerfectNC_000019.9:g.5594
    2255_55942877del
    GRCh37.p13First PassNC_000019.9Chr1955,942,25555,942,877

    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)
    nssv18049181<0.001638722
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