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nsv7031526

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,985

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 92 SVs from 23 studies. See in: genome view    
    Submitted genomic58,210,577-58,214,561Question Mark
    Overlapping variant regions from other studies: 92 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):56,785,633-56,789,617Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7031526Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2058,210,57758,214,561
    nsv7031526RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2056,785,63356,789,617

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18433930deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18433930Submitted genomicNC_000020.11:g.582
    10577_58214561del
    GRCh38 (hg38)NC_000020.11Chr2058,210,57758,214,561
    nssv18433930RemappedPerfectNC_000020.10:g.567
    85633_56789617del
    GRCh37.p13First PassNC_000020.10Chr2056,785,63356,789,617

    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)
    nssv184339304e-061276056
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