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nsv7059378

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,603,518

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 14257 SVs from 114 studies. See in: genome view    
    Submitted genomic87,626,566-93,230,083Question Mark
    Overlapping variant regions from other studies: 14211 SVs from 114 studies. See in: genome view    
    Remapped(Score: Good):88,092,910-93,674,575Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059378Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1487,626,56693,230,083
    nsv7059378RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1488,092,91093,674,575

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755283inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755283Submitted genomicNC_000014.9:g.8762
    6566_93230083inv
    GRCh38 (hg38)NC_000014.9Chr1487,626,56693,230,083
    nssv18755283RemappedGoodNC_000014.8:g.8809
    2910_93674575inv
    GRCh37.p13First PassNC_000014.8Chr1488,092,91093,674,575

    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)
    nssv187552834e-061276268
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