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nsv7067881

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:627,499

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1497 SVs from 78 studies. See in: genome view    
    Submitted genomic54,063,916-54,691,414Question Mark
    Overlapping variant regions from other studies: 1496 SVs from 78 studies. See in: genome view    
    Remapped(Score: Perfect):52,141,277-52,768,775Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067881Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1754,063,91654,691,414
    nsv7067881RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1752,141,27752,768,775

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757033inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757033Submitted genomicNC_000017.11:g.540
    63916_54691414inv
    GRCh38 (hg38)NC_000017.11Chr1754,063,91654,691,414
    nssv18757033RemappedPerfectNC_000017.10:g.521
    41277_52768775inv
    GRCh37.p13First PassNC_000017.10Chr1752,141,27752,768,775

    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)
    nssv187570334e-061276268
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