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nsv7058879

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,921,570

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6920 SVs from 115 studies. See in: genome view    
    Submitted genomic82,197,935-85,119,504Question Mark
    Overlapping variant regions from other studies: 7014 SVs from 115 studies. See in: genome view    
    Remapped(Score: Pass):82,490,276-85,662,735Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058879Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1582,197,93585,119,504
    nsv7058879RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1582,490,27685,662,735

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755165inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755165Submitted genomicNC_000015.10:g.821
    97935_85119504inv
    GRCh38 (hg38)NC_000015.10Chr1582,197,93585,119,504
    nssv18755165RemappedPassNC_000015.9:g.8249
    0276_85662735inv
    GRCh37.p13First PassNC_000015.9Chr1582,490,27685,662,735

    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)
    nssv187551654e-061276268
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