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nsv6586218

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,472,416

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 13566 SVs from 106 studies. See in: genome view    
    Submitted genomic107,936,497-114,408,912Question Mark
    Overlapping variant regions from other studies: 13571 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):107,807,223-114,279,634Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6586218Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11107,936,497114,408,912
    nsv6586218RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11107,807,223114,279,634

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18235855inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18235855Submitted genomicNC_000011.10:g.107
    936497_114408912in
    v
    GRCh38 (hg38)NC_000011.10Chr11107,936,497114,408,912
    nssv18235855RemappedPerfectNC_000011.9:g.1078
    07223_114279634inv
    GRCh37.p13First PassNC_000011.9Chr11107,807,223114,279,634

    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)
    nssv18235855<0.001139304
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