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nsv7055886

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,588,573

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3292 SVs from 105 studies. See in: genome view    
    Submitted genomic110,900,937-112,489,509Question Mark
    Overlapping variant regions from other studies: 3296 SVs from 105 studies. See in: genome view    
    Remapped(Score: Perfect):110,236,636-111,825,206Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055886Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5110,900,937112,489,509
    nsv7055886RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5110,236,636111,825,206

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774422inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774422Submitted genomicNC_000005.10:g.110
    900937_112489509in
    v
    GRCh38 (hg38)NC_000005.10Chr5110,900,937112,489,509
    nssv18774422RemappedPerfectNC_000005.9:g.1102
    36636_111825206inv
    GRCh37.p13First PassNC_000005.9Chr5110,236,636111,825,206

    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)
    nssv187744224e-061276268
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