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nsv7077621

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:231,748

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 907 SVs from 74 studies. See in: genome view    
    Submitted genomic112,105,538-112,337,285Question Mark
    Overlapping variant regions from other studies: 907 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):114,867,818-115,099,565Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077621Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9112,105,538112,337,285
    nsv7077621RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9114,867,818115,099,565

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783854inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783854Submitted genomicNC_000009.12:g.112
    105538_112337285in
    v
    GRCh38 (hg38)NC_000009.12Chr9112,105,538112,337,285
    nssv18783854RemappedPerfectNC_000009.11:g.114
    867818_115099565in
    v
    GRCh37.p13First PassNC_000009.11Chr9114,867,818115,099,565

    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)
    nssv187838544e-061276266
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