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nsv6540138

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:91

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 80 SVs from 16 studies. See in: genome view    
    Submitted genomic101,480,254-101,480,344Question Mark
    Overlapping variant regions from other studies: 80 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):101,199,098-101,199,188Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6540138Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3101,480,254101,480,344
    nsv6540138RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3101,199,098101,199,188

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18259469inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18259469Submitted genomicNC_000003.12:g.101
    480254_101480344in
    v
    GRCh38 (hg38)NC_000003.12Chr3101,480,254101,480,344
    nssv18259469RemappedPerfectNC_000003.11:g.101
    199098_101199188in
    v
    GRCh37.p13First PassNC_000003.11Chr3101,199,098101,199,188

    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)
    nssv18259469<0.001139304
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