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nsv7077538

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,146,150

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9930 SVs from 107 studies. See in: genome view    
    Submitted genomic63,703,374-67,849,523Question Mark
    Overlapping variant regions from other studies: 9933 SVs from 107 studies. See in: genome view    
    Remapped(Score: Perfect):64,170,092-68,316,240Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077538Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1463,703,37467,849,523
    nsv7077538RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1464,170,09268,316,240

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753918inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753918Submitted genomicNC_000014.9:g.6370
    3374_67849523inv
    GRCh38 (hg38)NC_000014.9Chr1463,703,37467,849,523
    nssv18753918RemappedPerfectNC_000014.8:g.6417
    0092_68316240inv
    GRCh37.p13First PassNC_000014.8Chr1464,170,09268,316,240

    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)
    nssv18753918<0.00129268750
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