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nsv7041760

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,848

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view    
    Submitted genomic98,032,764-98,034,611Question Mark
    Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):98,498,320-98,500,167Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7041760Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr198,032,76498,034,611
    nsv7041760RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr198,498,32098,500,167

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761510inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761510Submitted genomicNC_000001.11:g.980
    32764_98034611inv
    GRCh38 (hg38)NC_000001.11Chr198,032,76498,034,611
    nssv18761510RemappedPerfectNC_000001.10:g.984
    98320_98500167inv
    GRCh37.p13First PassNC_000001.10Chr198,498,32098,500,167

    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)
    nssv187615101.1e-053274606
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