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nsv7059147

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:106,207

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 367 SVs from 49 studies. See in: genome view    
    Submitted genomic21,659,104-21,765,310Question Mark
    Overlapping variant regions from other studies: 367 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):21,812,038-21,918,244Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059147Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1221,659,10421,765,310
    nsv7059147RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1221,812,03821,918,244

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18751170inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18751170Submitted genomicNC_000012.12:g.216
    59104_21765310inv
    GRCh38 (hg38)NC_000012.12Chr1221,659,10421,765,310
    nssv18751170RemappedPerfectNC_000012.11:g.218
    12038_21918244inv
    GRCh37.p13First PassNC_000012.11Chr1221,812,03821,918,244

    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)
    nssv187511701.8e-055274946
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