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nsv7075742

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:99

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 22 studies. See in: genome view    
    Submitted genomic13,625,374-13,625,472Question Mark
    Overlapping variant regions from other studies: 123 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):13,778,308-13,778,406Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7075742Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1213,625,37413,625,472
    nsv7075742RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1213,778,30813,778,406

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752192inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752192Submitted genomicNC_000012.12:g.136
    25374_13625472inv
    GRCh38 (hg38)NC_000012.12Chr1213,625,37413,625,472
    nssv18752192RemappedPerfectNC_000012.11:g.137
    78308_13778406inv
    GRCh37.p13First PassNC_000012.11Chr1213,778,30813,778,406

    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)
    nssv187521924e-061276268
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