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nsv6973285

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:321,511

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1208 SVs from 91 studies. See in: genome view    
    Submitted genomic85,990,173-86,311,683Question Mark
    Overlapping variant regions from other studies: 1208 SVs from 91 studies. See in: genome view    
    Remapped(Score: Perfect):86,456,517-86,778,027Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6973285Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1485,990,17386,311,683
    nsv6973285RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1486,456,51786,778,027

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18391503deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18391503Submitted genomicNC_000014.9:g.8599
    0173_86311683del
    GRCh38 (hg38)NC_000014.9Chr1485,990,17386,311,683
    nssv18391503RemappedPerfectNC_000014.8:g.8645
    6517_86778027del
    GRCh37.p13First PassNC_000014.8Chr1486,456,51786,778,027

    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)
    nssv183915032.8e-058275602
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