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nsv7067940

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:199

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 315 SVs from 28 studies. See in: genome view    
    Submitted genomic69,476,368-69,476,566Question Mark
    Overlapping variant regions from other studies: 315 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):67,143,604-67,143,802Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067940Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1869,476,36869,476,566
    nsv7067940RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1867,143,60467,143,802

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758886inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758886Submitted genomicNC_000018.10:g.694
    76368_69476566inv
    GRCh38 (hg38)NC_000018.10Chr1869,476,36869,476,566
    nssv18758886RemappedPerfectNC_000018.9:g.6714
    3604_67143802inv
    GRCh37.p13First PassNC_000018.9Chr1867,143,60467,143,802

    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)
    nssv187588860.002464274174
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