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nsv7051783

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,830

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 133 SVs from 35 studies. See in: genome view    
    Submitted genomic75,524,259-75,536,088Question Mark
    Overlapping variant regions from other studies: 133 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):76,449,469-76,461,298Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051783Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr475,524,25975,536,088
    nsv7051783RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr476,449,46976,461,298

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775672inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775672Submitted genomicNC_000004.12:g.755
    24259_75536088inv
    GRCh38 (hg38)NC_000004.12Chr475,524,25975,536,088
    nssv18775672RemappedPerfectNC_000004.11:g.764
    49469_76461298inv
    GRCh37.p13First PassNC_000004.11Chr476,449,46976,461,298

    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)
    nssv187756724e-061276268
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