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nsv7067668

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,306

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 29 studies. See in: genome view    
    Submitted genomic20,196,129-20,199,434Question Mark
    Overlapping variant regions from other studies: 85 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):20,664,288-20,667,593Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067668Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1420,196,12920,199,434
    nsv7067668RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1420,664,28820,667,593

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754270inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754270Submitted genomicNC_000014.9:g.2019
    6129_20199434inv
    GRCh38 (hg38)NC_000014.9Chr1420,196,12920,199,434
    nssv18754270RemappedPerfectNC_000014.8:g.2066
    4288_20667593inv
    GRCh37.p13First PassNC_000014.8Chr1420,664,28820,667,593

    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)
    nssv187542704e-061276268
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