U.S. flag

An official website of the United States government

nsv6737780

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:280

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 204 SVs from 24 studies. See in: genome view    
    Submitted genomic5,640,171-5,640,450Question Mark
    Overlapping variant regions from other studies: 204 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):5,641,898-5,642,177Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6737780Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr45,640,1715,640,450
    nsv6737780RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr45,641,8985,642,177

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18692856duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18692856Submitted genomicNC_000004.12:g.564
    0171_5640450dup
    GRCh38 (hg38)NC_000004.12Chr45,640,1715,640,450
    nssv18692856RemappedPerfectNC_000004.11:g.564
    1898_5642177dup
    GRCh37.p13First PassNC_000004.11Chr45,641,8985,642,177

    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)
    nssv186928561.7e-054229996
    Support Center