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nsv7040216

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,663

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 226 SVs from 50 studies. See in: genome view    
    Submitted genomic68,065,277-68,078,939Question Mark
    Overlapping variant regions from other studies: 226 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):68,930,995-68,944,657Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7040216Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr468,065,27768,078,939
    nsv7040216RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,930,99568,944,657

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775541inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775541Submitted genomicNC_000004.12:g.680
    65277_68078939inv
    GRCh38 (hg38)NC_000004.12Chr468,065,27768,078,939
    nssv18775541RemappedPerfectNC_000004.11:g.689
    30995_68944657inv
    GRCh37.p13First PassNC_000004.11Chr468,930,99568,944,657

    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)
    nssv187755414e-061276268
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