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nsv7048036

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,042,036

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2895 SVs from 93 studies. See in: genome view    
    Submitted genomic25,582,347-26,624,382Question Mark
    Overlapping variant regions from other studies: 2896 SVs from 93 studies. See in: genome view    
    Remapped(Score: Perfect):25,908,838-26,950,873Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048036Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr125,582,34726,624,382
    nsv7048036RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr125,908,83826,950,873

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760200inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760200Submitted genomicNC_000001.11:g.255
    82347_26624382inv
    GRCh38 (hg38)NC_000001.11Chr125,582,34726,624,382
    nssv18760200RemappedPerfectNC_000001.10:g.259
    08838_26950873inv
    GRCh37.p13First PassNC_000001.10Chr125,908,83826,950,873

    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)
    nssv187602000.003763272506
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