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nsv7047594

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:79,165

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1014 SVs from 97 studies. See in: genome view    
    Submitted genomic69,203,664-69,282,828Question Mark
    Overlapping variant regions from other studies: 1014 SVs from 97 studies. See in: genome view    
    Remapped(Score: Perfect):70,069,382-70,148,546Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047594Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr469,203,66469,282,828
    nsv7047594RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr470,069,38270,148,546

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775567inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775567Submitted genomicNC_000004.12:g.692
    03664_69282828inv
    GRCh38 (hg38)NC_000004.12Chr469,203,66469,282,828
    nssv18775567RemappedPerfectNC_000004.11:g.700
    69382_70148546inv
    GRCh37.p13First PassNC_000004.11Chr470,069,38270,148,546

    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)
    nssv18775567<0.00151274730
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