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nsv6969260

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,042

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 229 SVs from 29 studies. See in: genome view    
    Submitted genomic1,647,327-1,650,368Question Mark
    Overlapping variant regions from other studies: 229 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):1,697,328-1,700,369Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6969260Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr161,647,3271,650,368
    nsv6969260RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr161,697,3281,700,369

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18399319deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18399319Submitted genomicNC_000016.10:g.164
    7327_1650368del
    GRCh38 (hg38)NC_000016.10Chr161,647,3271,650,368
    nssv18399319RemappedPerfectNC_000016.9:g.1697
    328_1700369del
    GRCh37.p13First PassNC_000016.9Chr161,697,3281,700,369

    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)
    nssv183993194e-061271924
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