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nsv6962290

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:710,048

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2469 SVs from 87 studies. See in: genome view    
    Submitted genomic5,927,827-6,637,874Question Mark
    Overlapping variant regions from other studies: 2469 SVs from 87 studies. See in: genome view    
    Remapped(Score: Perfect):5,977,828-6,687,875Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6962290Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr165,927,8276,637,874
    nsv6962290RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr165,977,8286,687,875

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18621750duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18621750Submitted genomicNC_000016.10:g.592
    7827_6637874dup
    GRCh38 (hg38)NC_000016.10Chr165,927,8276,637,874
    nssv18621750RemappedPerfectNC_000016.9:g.5977
    828_6687875dup
    GRCh37.p13First PassNC_000016.9Chr165,977,8286,687,875

    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)
    nssv186217504e-061275860
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