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nsv7077127

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:154,604

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 493 SVs from 52 studies. See in: genome view    
    Submitted genomic26,819,519-26,974,122Question Mark
    Overlapping variant regions from other studies: 499 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):26,819,517-26,974,120Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077127Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr926,819,51926,974,122
    nsv7077127RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr926,819,51726,974,120

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18784604inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18784604Submitted genomicNC_000009.12:g.268
    19519_26974122inv
    GRCh38 (hg38)NC_000009.12Chr926,819,51926,974,122
    nssv18784604RemappedPerfectNC_000009.11:g.268
    19517_26974120inv
    GRCh37.p13First PassNC_000009.11Chr926,819,51726,974,120

    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)
    nssv187846044e-061276268
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