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nsv6923869

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 90 SVs from 16 studies. See in: genome view    
    Submitted genomic30,804,134-30,804,168Question Mark
    Overlapping variant regions from other studies: 90 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):31,378,271-31,378,305Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6923869Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1330,804,13430,804,168
    nsv6923869RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1331,378,27131,378,305

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18377122deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18377122Submitted genomicNC_000013.11:g.308
    04134_30804168del
    GRCh38 (hg38)NC_000013.11Chr1330,804,13430,804,168
    nssv18377122RemappedPerfectNC_000013.10:g.313
    78271_31378305del
    GRCh37.p13First PassNC_000013.10Chr1331,378,27131,378,305

    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)
    nssv183771224e-061266446
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