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nsv7059644

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,149,795

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4748 SVs from 113 studies. See in: genome view    
    Submitted genomic82,398,536-84,548,330Question Mark
    Overlapping variant regions from other studies: 4878 SVs from 113 studies. See in: genome view    
    Remapped(Score: Pass):82,690,748-85,091,561Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059644Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1582,398,53684,548,330
    nsv7059644RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1582,690,74885,091,561

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755177inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755177Submitted genomicNC_000015.10:g.823
    98536_84548330inv
    GRCh38 (hg38)NC_000015.10Chr1582,398,53684,548,330
    nssv18755177RemappedPassNC_000015.9:g.8269
    0748_85091561inv
    GRCh37.p13First PassNC_000015.9Chr1582,690,74885,091,561

    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)
    nssv18755177<0.00142273078
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