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nsv7076578

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:290,555

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1361 SVs from 87 studies. See in: genome view    
    Submitted genomic83,742,713-84,033,267Question Mark
    Overlapping variant regions from other studies: 1361 SVs from 87 studies. See in: genome view    
    Remapped(Score: Perfect):83,776,318-84,066,872Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7076578Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1683,742,71384,033,267
    nsv7076578RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1683,776,31884,066,872

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756629inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756629Submitted genomicNC_000016.10:g.837
    42713_84033267inv
    GRCh38 (hg38)NC_000016.10Chr1683,742,71384,033,267
    nssv18756629RemappedPerfectNC_000016.9:g.8377
    6318_84066872inv
    GRCh37.p13First PassNC_000016.9Chr1683,776,31884,066,872

    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)
    nssv187566294e-061276268
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