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nsv7051894

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,761,570

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8060 SVs from 106 studies. See in: genome view    
    Submitted genomic245,875,322-247,636,891Question Mark
    Overlapping variant regions from other studies: 8063 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):246,038,624-247,800,193Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051894Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1245,875,322247,636,891
    nsv7051894RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1246,038,624247,800,193

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759471inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759471Submitted genomicNC_000001.11:g.245
    875322_247636891in
    v
    GRCh38 (hg38)NC_000001.11Chr1245,875,322247,636,891
    nssv18759471RemappedPerfectNC_000001.10:g.246
    038624_247800193in
    v
    GRCh37.p13First PassNC_000001.10Chr1246,038,624247,800,193

    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)
    nssv187594711.4e-054274256
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