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nsv6970199

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 139 SVs from 29 studies. See in: genome view    
    Submitted genomic55,407,601-55,409,100Question Mark
    Overlapping variant regions from other studies: 139 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):55,699,799-55,701,298Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6970199Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1555,407,60155,409,100
    nsv6970199RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1555,699,79955,701,298

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18617317duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18617317Submitted genomicNC_000015.10:g.554
    07601_55409100dup
    GRCh38 (hg38)NC_000015.10Chr1555,407,60155,409,100
    nssv18617317RemappedPerfectNC_000015.9:g.5569
    9799_55701298dup
    GRCh37.p13First PassNC_000015.9Chr1555,699,79955,701,298

    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)
    nssv186173174e-061240800
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