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nsv7048381

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,615

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 386 SVs from 66 studies. See in: genome view    
    Submitted genomic189,482,151-189,487,765Question Mark
    Overlapping variant regions from other studies: 386 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):189,451,281-189,456,895Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048381Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1189,482,151189,487,765
    nsv7048381RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1189,451,281189,456,895

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18736898inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18736898Submitted genomicNC_000001.11:g.189
    482151_189487765in
    v
    GRCh38 (hg38)NC_000001.11Chr1189,482,151189,487,765
    nssv18736898RemappedPerfectNC_000001.10:g.189
    451281_189456895in
    v
    GRCh37.p13First PassNC_000001.10Chr1189,451,281189,456,895

    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)
    nssv187368984e-061276266
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