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nsv6970342

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,170

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 190 SVs from 48 studies. See in: genome view    
    Submitted genomic4,086,237-4,095,406Question Mark
    Overlapping variant regions from other studies: 190 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):4,136,238-4,145,407Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6970342Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr164,086,2374,095,406
    nsv6970342RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr164,136,2384,145,407

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18623474duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18623474Submitted genomicNC_000016.10:g.408
    6237_4095406dup
    GRCh38 (hg38)NC_000016.10Chr164,086,2374,095,406
    nssv18623474RemappedPerfectNC_000016.9:g.4136
    238_4145407dup
    GRCh37.p13First PassNC_000016.9Chr164,136,2384,145,407

    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)
    nssv186234744e-061275752
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