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nsv6563691

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:797

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 19 studies. See in: genome view    
    Submitted genomic141,810,528-141,811,324Question Mark
    Overlapping variant regions from other studies: 101 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):141,529,370-141,530,166Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6563691Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3141,810,528141,811,324
    nsv6563691RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3141,529,370141,530,166

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18259783inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18259783Submitted genomicNC_000003.12:g.141
    810528_141811324in
    v
    GRCh38 (hg38)NC_000003.12Chr3141,810,528141,811,324
    nssv18259783RemappedPerfectNC_000003.11:g.141
    529370_141530166in
    v
    GRCh37.p13First PassNC_000003.11Chr3141,529,370141,530,166

    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)
    nssv18259783<0.001136696
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