U.S. flag

An official website of the United States government

nsv7019769

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:352,028

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1161 SVs from 73 studies. See in: genome view    
    Submitted genomic33,313,823-33,665,850Question Mark
    Overlapping variant regions from other studies: 1161 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):31,901,629-32,253,656Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7019769Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2033,313,82333,665,850
    nsv7019769RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2031,901,62932,253,656

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18642004duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18642004Submitted genomicNC_000020.11:g.333
    13823_33665850dup
    GRCh38 (hg38)NC_000020.11Chr2033,313,82333,665,850
    nssv18642004RemappedPerfectNC_000020.10:g.319
    01629_32253656dup
    GRCh37.p13First PassNC_000020.10Chr2031,901,62932,253,656

    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)
    nssv186420044e-061274838
    Support Center