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nsv6590616

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:504

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 20 studies. See in: genome view    
    Submitted genomic113,919,799-113,920,302Question Mark
    Overlapping variant regions from other studies: 94 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):113,790,521-113,791,024Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6590616Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11113,919,799113,920,302
    nsv6590616RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11113,790,521113,791,024

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18224545inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18224545Submitted genomicNC_000011.10:g.113
    919799_113920302in
    v
    GRCh38 (hg38)NC_000011.10Chr11113,919,799113,920,302
    nssv18224545RemappedPerfectNC_000011.9:g.1137
    90521_113791024inv
    GRCh37.p13First PassNC_000011.9Chr11113,790,521113,791,024

    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)
    nssv18224545<0.0011533366
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