U.S. flag

An official website of the United States government

nsv6660567

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:873,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2930 SVs from 91 studies. See in: genome view    
    Submitted genomic234,838,301-235,712,200Question Mark
    Overlapping variant regions from other studies: 2919 SVs from 91 studies. See in: genome view    
    Remapped(Score: Good):234,974,048-235,875,500Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6660567Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1234,838,301235,712,200
    nsv6660567RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1234,974,048235,875,500

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18608063duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18608063Submitted genomicNC_000001.11:g.234
    838301_235712200du
    p
    GRCh38 (hg38)NC_000001.11Chr1234,838,301235,712,200
    nssv18608063RemappedGoodNC_000001.10:g.234
    974048_235875500du
    p
    GRCh37.p13First PassNC_000001.10Chr1234,974,048235,875,500

    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)
    nssv186080634e-061268072
    Support Center