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nsv6558908

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:518

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 92 SVs from 20 studies. See in: genome view    
    Submitted genomic111,537,891-111,538,408Question Mark
    Overlapping variant regions from other studies: 92 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):114,300,171-114,300,688Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6558908Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9111,537,891111,538,408
    nsv6558908RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9114,300,171114,300,688

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18279550inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18279550Submitted genomicNC_000009.12:g.111
    537891_111538408in
    v
    GRCh38 (hg38)NC_000009.12Chr9111,537,891111,538,408
    nssv18279550RemappedPerfectNC_000009.11:g.114
    300171_114300688in
    v
    GRCh37.p13First PassNC_000009.11Chr9114,300,171114,300,688

    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)
    nssv18279550<0.001236134
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