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nsv7017449

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:122,452

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 510 SVs from 63 studies. See in: genome view    
    Submitted genomic58,292,208-58,414,659Question Mark
    Overlapping variant regions from other studies: 512 SVs from 63 studies. See in: genome view    
    Remapped(Score: Good):58,803,574-58,926,026Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7017449Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1958,292,20858,414,659
    nsv7017449RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1958,803,57458,926,026

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18640311duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18640311Submitted genomicNC_000019.10:g.582
    92208_58414659dup
    GRCh38 (hg38)NC_000019.10Chr1958,292,20858,414,659
    nssv18640311RemappedGoodNC_000019.9:g.5880
    3574_58926026dup
    GRCh37.p13First PassNC_000019.9Chr1958,803,57458,926,026

    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)
    nssv186403114e-061275670
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