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nsv7046317

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,353

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 141 SVs from 28 studies. See in: genome view    
    Submitted genomic57,505,378-57,525,730Question Mark
    Overlapping variant regions from other studies: 141 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):57,971,050-57,991,402Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7046317Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr157,505,37857,525,730
    nsv7046317RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr157,971,05057,991,402

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761609inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761609Submitted genomicNC_000001.11:g.575
    05378_57525730inv
    GRCh38 (hg38)NC_000001.11Chr157,505,37857,525,730
    nssv18761609RemappedPerfectNC_000001.10:g.579
    71050_57991402inv
    GRCh37.p13First PassNC_000001.10Chr157,971,05057,991,402

    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)
    nssv187616094e-061276262
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