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nsv7057253

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57,405

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 356 SVs from 64 studies. See in: genome view    
    Submitted genomic29,095,695-29,153,099Question Mark
    Overlapping variant regions from other studies: 356 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):29,063,472-29,120,876Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057253Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr629,095,69529,153,099
    nsv7057253RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr629,063,47229,120,876

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18778545inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18778545Submitted genomicNC_000006.12:g.290
    95695_29153099inv
    GRCh38 (hg38)NC_000006.12Chr629,095,69529,153,099
    nssv18778545RemappedPerfectNC_000006.11:g.290
    63472_29120876inv
    GRCh37.p13First PassNC_000006.11Chr629,063,47229,120,876

    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)
    nssv187785454e-061276268
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