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nsv6573167

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:585

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 24 studies. See in: genome view    
    Submitted genomic112,381,377-112,381,961Question Mark
    Overlapping variant regions from other studies: 94 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):115,143,657-115,144,241Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6573167Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9112,381,377112,381,961
    nsv6573167RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9115,143,657115,144,241

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18279595inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18279595Submitted genomicNC_000009.12:g.112
    381377_112381961in
    v
    GRCh38 (hg38)NC_000009.12Chr9112,381,377112,381,961
    nssv18279595RemappedPerfectNC_000009.11:g.115
    143657_115144241in
    v
    GRCh37.p13First PassNC_000009.11Chr9115,143,657115,144,241

    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)
    nssv18279595<0.001236632
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