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nsv7066137

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,557,129

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4910 SVs from 104 studies. See in: genome view    
    Submitted genomic43,668,049-45,225,177Question Mark
    Overlapping variant regions from other studies: 4938 SVs from 104 studies. See in: genome view    
    Remapped(Score: Good):44,172,201-45,728,435Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066137Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1943,668,04945,225,177
    nsv7066137RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1944,172,20145,728,435

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760776inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760776Submitted genomicNC_000019.10:g.436
    68049_45225177inv
    GRCh38 (hg38)NC_000019.10Chr1943,668,04945,225,177
    nssv18760776RemappedGoodNC_000019.9:g.4417
    2201_45728435inv
    GRCh37.p13First PassNC_000019.9Chr1944,172,20145,728,435

    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)
    nssv187607761.4e-054273678
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