U.S. flag

An official website of the United States government

nsv6326024

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:400,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1914 SVs from 94 studies. See in: genome view    
    Submitted genomic189,192,501-189,593,400Question Mark
    Overlapping variant regions from other studies: 1914 SVs from 94 studies. See in: genome view    
    Remapped(Score: Perfect):189,161,632-189,562,530Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6326024Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1189,192,501189,593,400
    nsv6326024RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1189,161,632189,562,530

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18199169duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18199169Submitted genomicNC_000001.11:g.189
    192501_189593400du
    p
    GRCh38 (hg38)NC_000001.11Chr1189,192,501189,593,400
    nssv18199169RemappedPerfectNC_000001.10:g.189
    161632_189562530du
    p
    GRCh37.p13First PassNC_000001.10Chr1189,161,632189,562,530

    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)
    nssv18199169<0.001138320
    Support Center