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nsv7059316

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,803,762

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 16638 SVs from 116 studies. See in: genome view    
    Submitted genomic43,396,877-48,200,638Question Mark
    Overlapping variant regions from other studies: 16667 SVs from 116 studies. See in: genome view    
    Remapped(Score: Good):43,901,029-48,703,895Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059316Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1943,396,87748,200,638
    nsv7059316RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1943,901,02948,703,895

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760770inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760770Submitted genomicNC_000019.10:g.433
    96877_48200638inv
    GRCh38 (hg38)NC_000019.10Chr1943,396,87748,200,638
    nssv18760770RemappedGoodNC_000019.9:g.4390
    1029_48703895inv
    GRCh37.p13First PassNC_000019.9Chr1943,901,02948,703,895

    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)
    nssv187607704e-061276268
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