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nsv7067755

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:105

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 87 SVs from 14 studies. See in: genome view    
    Submitted genomic48,756,054-48,756,158Question Mark
    Overlapping variant regions from other studies: 87 SVs from 14 studies. See in: genome view    
    Remapped(Score: Perfect):47,372,591-47,372,695Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067755Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2048,756,05448,756,158
    nsv7067755RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2047,372,59147,372,695

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761801inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761801Submitted genomicNC_000020.11:g.487
    56054_48756158inv
    GRCh38 (hg38)NC_000020.11Chr2048,756,05448,756,158
    nssv18761801RemappedPerfectNC_000020.10:g.473
    72591_47372695inv
    GRCh37.p13First PassNC_000020.10Chr2047,372,59147,372,695

    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)
    nssv187618014e-061276244
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