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nsv7069168

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,920,502

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5263 SVs from 93 studies. See in: genome view    
    Submitted genomic65,085,774-67,006,275Question Mark
    Overlapping variant regions from other studies: 5263 SVs from 93 studies. See in: genome view    
    Remapped(Score: Perfect):65,378,112-67,298,613Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7069168Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1565,085,77467,006,275
    nsv7069168RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1565,378,11267,298,613

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755752inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755752Submitted genomicNC_000015.10:g.650
    85774_67006275inv
    GRCh38 (hg38)NC_000015.10Chr1565,085,77467,006,275
    nssv18755752RemappedPerfectNC_000015.9:g.6537
    8112_67298613inv
    GRCh37.p13First PassNC_000015.9Chr1565,378,11267,298,613

    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)
    nssv187557524e-061276268
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