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nsv6579765

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,152

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 91 SVs from 17 studies. See in: genome view    
    Submitted genomic117,283,654-117,284,805Question Mark
    Overlapping variant regions from other studies: 91 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):117,154,370-117,155,521Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6579765Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11117,283,654117,284,805
    nsv6579765RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11117,154,370117,155,521

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18235475inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18235475Submitted genomicNC_000011.10:g.117
    283654_117284805in
    v
    GRCh38 (hg38)NC_000011.10Chr11117,283,654117,284,805
    nssv18235475RemappedPerfectNC_000011.9:g.1171
    54370_117155521inv
    GRCh37.p13First PassNC_000011.9Chr11117,154,370117,155,521

    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)
    nssv18235475<0.001136058
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