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nsv6597167

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,479,932

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9357 SVs from 106 studies. See in: genome view    
    Submitted genomic55,930,699-58,410,630Question Mark
    Overlapping variant regions from other studies: 9359 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):56,442,065-58,921,997Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6597167Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1955,930,69958,410,630
    nsv6597167RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1956,442,06558,921,997

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18248497inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18248497Submitted genomicNC_000019.10:g.559
    30699_58410630inv
    GRCh38 (hg38)NC_000019.10Chr1955,930,69958,410,630
    nssv18248497RemappedPerfectNC_000019.9:g.5644
    2065_58921997inv
    GRCh37.p13First PassNC_000019.9Chr1956,442,06558,921,997

    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)
    nssv182484970.0026431582
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