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nsv7059381

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:113,151

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 684 SVs from 73 studies. See in: genome view    
    Submitted genomic84,882,337-84,995,487Question Mark
    Overlapping variant regions from other studies: 684 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):85,425,568-85,538,718Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059381Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1584,882,33784,995,487
    nsv7059381RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1585,425,56885,538,718

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755211inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755211Submitted genomicNC_000015.10:g.848
    82337_84995487inv
    GRCh38 (hg38)NC_000015.10Chr1584,882,33784,995,487
    nssv18755211RemappedPerfectNC_000015.9:g.8542
    5568_85538718inv
    GRCh37.p13First PassNC_000015.9Chr1585,425,56885,538,718

    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)
    nssv187552114e-061276268
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