U.S. flag

An official website of the United States government

nsv6734371

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:712,698

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1407 SVs from 71 studies. See in: genome view    
    Submitted genomic156,578,264-157,290,961Question Mark
    Overlapping variant regions from other studies: 1407 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):156,296,053-157,008,750Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6734371Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3156,578,264157,290,961
    nsv6734371RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3156,296,053157,008,750

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18672518duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18672518Submitted genomicNC_000003.12:g.156
    578264_157290961du
    p
    GRCh38 (hg38)NC_000003.12Chr3156,578,264157,290,961
    nssv18672518RemappedPerfectNC_000003.11:g.156
    296053_157008750du
    p
    GRCh37.p13First PassNC_000003.11Chr3156,296,053157,008,750

    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)
    nssv186725184e-061275488
    Support Center