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nsv7069678

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:111,556

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 492 SVs from 65 studies. See in: genome view    
    Submitted genomic26,899,186-27,010,741Question Mark
    Overlapping variant regions from other studies: 492 SVs from 65 studies. See in: genome view    
    Remapped(Score: Perfect):24,479,150-24,590,705Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7069678Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1826,899,18627,010,741
    nsv7069678RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1824,479,15024,590,705

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758824inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758824Submitted genomicNC_000018.10:g.268
    99186_27010741inv
    GRCh38 (hg38)NC_000018.10Chr1826,899,18627,010,741
    nssv18758824RemappedPerfectNC_000018.9:g.2447
    9150_24590705inv
    GRCh37.p13First PassNC_000018.9Chr1824,479,15024,590,705

    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)
    nssv187588244e-061276268
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