U.S. flag

An official website of the United States government

nsv7035934

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:236,693

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1664 SVs from 84 studies. See in: genome view    
    Submitted genomic50,316,944-50,553,636Question Mark
    Overlapping variant regions from other studies: 1664 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):50,755,373-50,992,065Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7035934Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2250,316,94450,553,636
    nsv7035934RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2250,755,37350,992,065

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18652646duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18652646Submitted genomicNC_000022.11:g.503
    16944_50553636dup
    GRCh38 (hg38)NC_000022.11Chr2250,316,94450,553,636
    nssv18652646RemappedPerfectNC_000022.10:g.507
    55373_50992065dup
    GRCh37.p13First PassNC_000022.10Chr2250,755,37350,992,065

    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)
    nssv186526464e-061275532
    Support Center