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nsv7050860

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:181,727

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 452 SVs from 58 studies. See in: genome view    
    Submitted genomic97,948,396-98,130,122Question Mark
    Overlapping variant regions from other studies: 452 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):98,564,859-98,746,585Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7050860Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr297,948,39698,130,122
    nsv7050860RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr298,564,85998,746,585

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18770079inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18770079Submitted genomicNC_000002.12:g.979
    48396_98130122inv
    GRCh38 (hg38)NC_000002.12Chr297,948,39698,130,122
    nssv18770079RemappedPerfectNC_000002.11:g.985
    64859_98746585inv
    GRCh37.p13First PassNC_000002.11Chr298,564,85998,746,585

    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)
    nssv187700797e-062274594
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