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nsv6986139

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 177 SVs from 49 studies. See in: genome view    
    Submitted genomic7,433,101-7,434,400Question Mark
    Overlapping variant regions from other studies: 177 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):7,336,420-7,337,719Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6986139Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr177,433,1017,434,400
    nsv6986139RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr177,336,4207,337,719

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18414213deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18414213Submitted genomicNC_000017.11:g.743
    3101_7434400del
    GRCh38 (hg38)NC_000017.11Chr177,433,1017,434,400
    nssv18414213RemappedPerfectNC_000017.10:g.733
    6420_7337719del
    GRCh37.p13First PassNC_000017.10Chr177,336,4207,337,719

    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)
    nssv184142130.06315825252968
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