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nsv6590111

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:319

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 189 SVs from 22 studies. See in: genome view    
    Submitted genomic130,325,020-130,325,338Question Mark
    Overlapping variant regions from other studies: 189 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):130,194,915-130,195,233Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6590111Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11130,325,020130,325,338
    nsv6590111RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11130,194,915130,195,233

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18223215inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18223215Submitted genomicNC_000011.10:g.130
    325020_130325338in
    v
    GRCh38 (hg38)NC_000011.10Chr11130,325,020130,325,338
    nssv18223215RemappedPerfectNC_000011.9:g.1301
    94915_130195233inv
    GRCh37.p13First PassNC_000011.9Chr11130,194,915130,195,233

    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)
    nssv18223215<0.001135756
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