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nsv7061118

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:587,888

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2428 SVs from 91 studies. See in: genome view    
    Submitted genomic20,936,120-21,524,007Question Mark
    Overlapping variant regions from other studies: 2428 SVs from 91 studies. See in: genome view    
    Remapped(Score: Perfect):21,510,259-22,098,146Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061118Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1320,936,12021,524,007
    nsv7061118RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1321,510,25922,098,146

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752840inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752840Submitted genomicNC_000013.11:g.209
    36120_21524007inv
    GRCh38 (hg38)NC_000013.11Chr1320,936,12021,524,007
    nssv18752840RemappedPerfectNC_000013.10:g.215
    10259_22098146inv
    GRCh37.p13First PassNC_000013.10Chr1321,510,25922,098,146

    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)
    nssv187528401.8e-055272236
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