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nsv6566343

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,275

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 124 SVs from 19 studies. See in: genome view    
    Submitted genomic115,861,712-115,862,986Question Mark
    Overlapping variant regions from other studies: 124 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):115,197,409-115,198,683Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6566343Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5115,861,712115,862,986
    nsv6566343RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5115,197,409115,198,683

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18266608inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18266608Submitted genomicNC_000005.10:g.115
    861712_115862986in
    v
    GRCh38 (hg38)NC_000005.10Chr5115,861,712115,862,986
    nssv18266608RemappedPerfectNC_000005.9:g.1151
    97409_115198683inv
    GRCh37.p13First PassNC_000005.9Chr5115,197,409115,198,683

    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)
    nssv18266608<0.001139304
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