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nsv6980804

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:125,361

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 735 SVs from 70 studies. See in: genome view    
    Submitted genomic40,949,294-41,074,654Question Mark
    Overlapping variant regions from other studies: 733 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):39,105,546-39,230,906Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6980804Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1740,949,29441,074,654
    nsv6980804RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1739,105,54639,230,906

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18407269deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18407269Submitted genomicNC_000017.11:g.409
    49294_41074654del
    GRCh38 (hg38)NC_000017.11Chr1740,949,29441,074,654
    nssv18407269RemappedPerfectNC_000017.10:g.391
    05546_39230906del
    GRCh37.p13First PassNC_000017.10Chr1739,105,54639,230,906

    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)
    nssv184072694e-061276258
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