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nsv6980449

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 165 SVs from 33 studies. See in: genome view    
    Submitted genomic86,553,701-86,560,600Question Mark
    Overlapping variant regions from other studies: 165 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):86,587,307-86,594,206Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6980449Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1686,553,70186,560,600
    nsv6980449RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1686,587,30786,594,206

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18406492deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18406492Submitted genomicNC_000016.10:g.865
    53701_86560600del
    GRCh38 (hg38)NC_000016.10Chr1686,553,70186,560,600
    nssv18406492RemappedPerfectNC_000016.9:g.8658
    7307_86594206del
    GRCh37.p13First PassNC_000016.9Chr1686,587,30786,594,206

    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)
    nssv184064927.4e-0521276222
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