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nsv7073187

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:100,312

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 255 SVs from 58 studies. See in: genome view    
    Submitted genomic74,758,590-74,858,901Question Mark
    Overlapping variant regions from other studies: 255 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):74,469,635-74,569,946Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073187Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1174,758,59074,858,901
    nsv7073187RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1174,469,63574,569,946

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18731081inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18731081Submitted genomicNC_000011.10:g.747
    58590_74858901inv
    GRCh38 (hg38)NC_000011.10Chr1174,758,59074,858,901
    nssv18731081RemappedPerfectNC_000011.9:g.7446
    9635_74569946inv
    GRCh37.p13First PassNC_000011.9Chr1174,469,63574,569,946

    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)
    nssv187310813.9e-0511273846
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