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nsv6983431

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:141,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 596 SVs from 50 studies. See in: genome view    
    Submitted genomic51,059,401-51,201,300Question Mark
    Overlapping variant regions from other studies: 595 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):49,136,762-49,278,661Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6983431Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1751,059,40151,201,300
    nsv6983431RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1749,136,76249,278,661

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18626722duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18626722Submitted genomicNC_000017.11:g.510
    59401_51201300dup
    GRCh38 (hg38)NC_000017.11Chr1751,059,40151,201,300
    nssv18626722RemappedPerfectNC_000017.10:g.491
    36762_49278661dup
    GRCh37.p13First PassNC_000017.10Chr1749,136,76249,278,661

    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)
    nssv186267224e-061274886
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