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nsv7074919

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:101

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 21 studies. See in: genome view    
    Submitted genomic59,465,330-59,465,430Question Mark
    Overlapping variant regions from other studies: 108 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):59,757,529-59,757,629Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074919Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1559,465,33059,465,430
    nsv7074919RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1559,757,52959,757,629

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756325inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756325Submitted genomicNC_000015.10:g.594
    65330_59465430inv
    GRCh38 (hg38)NC_000015.10Chr1559,465,33059,465,430
    nssv18756325RemappedPerfectNC_000015.9:g.5975
    7529_59757629inv
    GRCh37.p13First PassNC_000015.9Chr1559,757,52959,757,629

    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)
    nssv18756325<0.001100273186
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