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nsv6972459

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:694,218

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2198 SVs from 81 studies. See in: genome view    
    Submitted genomic55,166,400-55,860,617Question Mark
    Overlapping variant regions from other studies: 2198 SVs from 81 studies. See in: genome view    
    Remapped(Score: Perfect):55,458,598-56,152,815Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6972459Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1555,166,40055,860,617
    nsv6972459RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1555,458,59856,152,815

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18617306duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18617306Submitted genomicNC_000015.10:g.551
    66400_55860617dup
    GRCh38 (hg38)NC_000015.10Chr1555,166,40055,860,617
    nssv18617306RemappedPerfectNC_000015.9:g.5545
    8598_56152815dup
    GRCh37.p13First PassNC_000015.9Chr1555,458,59856,152,815

    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)
    nssv186173064e-061275180
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