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nsv6998445

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:428

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 341 SVs from 19 studies. See in: genome view    
    Submitted genomic76,124,628-76,125,055Question Mark
    Overlapping variant regions from other studies: 341 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):73,836,583-73,837,010Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6998445Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1876,124,62876,125,055
    nsv6998445RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1873,836,58373,837,010

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18635025duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18635025Submitted genomicNC_000018.10:g.761
    24628_76125055dup
    GRCh38 (hg38)NC_000018.10Chr1876,124,62876,125,055
    nssv18635025RemappedPerfectNC_000018.9:g.7383
    6583_73837010dup
    GRCh37.p13First PassNC_000018.9Chr1873,836,58373,837,010

    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)
    nssv186350254e-061245016
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