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nsv6569908

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,522

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 89 SVs from 21 studies. See in: genome view    
    Submitted genomic122,659,568-122,661,089Question Mark
    Overlapping variant regions from other studies: 89 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):125,421,847-125,423,368Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6569908Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9122,659,568122,661,089
    nsv6569908RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9125,421,847125,423,368

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18279784inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18279784Submitted genomicNC_000009.12:g.122
    659568_122661089in
    v
    GRCh38 (hg38)NC_000009.12Chr9122,659,568122,661,089
    nssv18279784RemappedPerfectNC_000009.11:g.125
    421847_125423368in
    v
    GRCh37.p13First PassNC_000009.11Chr9125,421,847125,423,368

    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)
    nssv18279784<0.001135918
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