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nsv6563554

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,130,957

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 10824 SVs from 122 studies. See in: genome view    
    Submitted genomic126,481,307-130,612,263Question Mark
    Overlapping variant regions from other studies: 10826 SVs from 122 studies. See in: genome view    
    Remapped(Score: Perfect):126,200,150-130,331,107Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6563554Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3126,481,307130,612,263
    nsv6563554RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3126,200,150130,331,107

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18259569inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18259569Submitted genomicNC_000003.12:g.126
    481307_130612263in
    v
    GRCh38 (hg38)NC_000003.12Chr3126,481,307130,612,263
    nssv18259569RemappedPerfectNC_000003.11:g.126
    200150_130331107in
    v
    GRCh37.p13First PassNC_000003.11Chr3126,200,150130,331,107

    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)
    nssv18259569<0.001239304
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