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nsv7067794

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,829

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 133 SVs from 23 studies. See in: genome view    
    Submitted genomic92,695,597-92,697,425Question Mark
    Overlapping variant regions from other studies: 133 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):93,238,827-93,240,655Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067794Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1592,695,59792,697,425
    nsv7067794RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1593,238,82793,240,655

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756669inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756669Submitted genomicNC_000015.10:g.926
    95597_92697425inv
    GRCh38 (hg38)NC_000015.10Chr1592,695,59792,697,425
    nssv18756669RemappedPerfectNC_000015.9:g.9323
    8827_93240655inv
    GRCh37.p13First PassNC_000015.9Chr1593,238,82793,240,655

    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)
    nssv187566694e-061276268
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