U.S. flag

An official website of the United States government

nsv6990482

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:116,578

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 440 SVs from 51 studies. See in: genome view    
    Submitted genomic58,904,879-59,021,456Question Mark
    Overlapping variant regions from other studies: 439 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):56,982,240-57,098,817Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6990482Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1758,904,87959,021,456
    nsv6990482RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1756,982,24057,098,817

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18627306duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18627306Submitted genomicNC_000017.11:g.589
    04879_59021456dup
    GRCh38 (hg38)NC_000017.11Chr1758,904,87959,021,456
    nssv18627306RemappedPerfectNC_000017.10:g.569
    82240_57098817dup
    GRCh37.p13First PassNC_000017.10Chr1756,982,24057,098,817

    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)
    nssv186273062.1e-056274544
    Support Center