U.S. flag

An official website of the United States government

nsv6737359

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:756

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 19 studies. See in: genome view    
    Submitted genomic133,796,828-133,797,583Question Mark
    Overlapping variant regions from other studies: 85 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):133,515,672-133,516,427Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6737359Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3133,796,828133,797,583
    nsv6737359RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3133,515,672133,516,427

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18672171duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18672171Submitted genomicNC_000003.12:g.133
    796828_133797583du
    p
    GRCh38 (hg38)NC_000003.12Chr3133,796,828133,797,583
    nssv18672171RemappedPerfectNC_000003.11:g.133
    515672_133516427du
    p
    GRCh37.p13First PassNC_000003.11Chr3133,515,672133,516,427

    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)
    nssv186721718e-062247964
    Support Center