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nsv7042730

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,193

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 186 SVs from 44 studies. See in: genome view    
    Submitted genomic86,839,887-86,855,079Question Mark
    Overlapping variant regions from other studies: 186 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):87,761,040-87,776,232Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7042730Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr486,839,88786,855,079
    nsv7042730RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr487,761,04087,776,232

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18776430inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18776430Submitted genomicNC_000004.12:g.868
    39887_86855079inv
    GRCh38 (hg38)NC_000004.12Chr486,839,88786,855,079
    nssv18776430RemappedPerfectNC_000004.11:g.877
    61040_87776232inv
    GRCh37.p13First PassNC_000004.11Chr487,761,04087,776,232

    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)
    nssv187764301.1e-053276268
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