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nsv7053546

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:254,934

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 723 SVs from 63 studies. See in: genome view    
    Submitted genomic54,555,777-54,810,710Question Mark
    Overlapping variant regions from other studies: 723 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):55,421,944-55,676,876Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053546Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr454,555,77754,810,710
    nsv7053546RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr455,421,94455,676,876

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774749inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774749Submitted genomicNC_000004.12:g.545
    55777_54810710inv
    GRCh38 (hg38)NC_000004.12Chr454,555,77754,810,710
    nssv18774749RemappedPerfectNC_000004.11:g.554
    21944_55676876inv
    GRCh37.p13First PassNC_000004.11Chr455,421,94455,676,876

    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)
    nssv187747494e-061276268
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