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nsv7047217

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,101

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 19 studies. See in: genome view    
    Submitted genomic26,281,994-26,284,094Question Mark
    Overlapping variant regions from other studies: 118 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):26,282,222-26,284,322Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047217Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr626,281,99426,284,094
    nsv7047217RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr626,282,22226,284,322

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18778492inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18778492Submitted genomicNC_000006.12:g.262
    81994_26284094inv
    GRCh38 (hg38)NC_000006.12Chr626,281,99426,284,094
    nssv18778492RemappedPerfectNC_000006.11:g.262
    82222_26284322inv
    GRCh37.p13First PassNC_000006.11Chr626,282,22226,284,322

    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)
    nssv187784924e-061276224
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