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nsv7059555

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:979,267

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3028 SVs from 100 studies. See in: genome view    
    Submitted genomic84,402,911-85,382,177Question Mark
    Overlapping variant regions from other studies: 3022 SVs from 100 studies. See in: genome view    
    Remapped(Score: Good):84,957,609-85,925,408Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059555Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1584,402,91185,382,177
    nsv7059555RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1584,957,60985,925,408

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755202inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755202Submitted genomicNC_000015.10:g.844
    02911_85382177inv
    GRCh38 (hg38)NC_000015.10Chr1584,402,91185,382,177
    nssv18755202RemappedGoodNC_000015.9:g.8495
    7609_85925408inv
    GRCh37.p13First PassNC_000015.9Chr1584,957,60985,925,408

    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)
    nssv187552024e-061276266
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