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nsv6998518

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 451 SVs from 66 studies. See in: genome view    
    Submitted genomic36,341,401-36,378,100Question Mark
    Overlapping variant regions from other studies: 451 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):36,832,303-36,869,002Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6998518Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,341,40136,378,100
    nsv6998518RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,832,30336,869,002

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18637855duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18637855Submitted genomicNC_000019.10:g.363
    41401_36378100dup
    GRCh38 (hg38)NC_000019.10Chr1936,341,40136,378,100
    nssv18637855RemappedPerfectNC_000019.9:g.3683
    2303_36869002dup
    GRCh37.p13First PassNC_000019.9Chr1936,832,30336,869,002

    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)
    nssv186378554e-061273894
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