U.S. flag

An official website of the United States government

nsv6704743

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:504,174

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1143 SVs from 71 studies. See in: genome view    
    Submitted genomic113,082,325-113,586,498Question Mark
    Overlapping variant regions from other studies: 1143 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):112,801,172-113,305,345Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6704743Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3113,082,325113,586,498
    nsv6704743RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3112,801,172113,305,345

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18668023duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18668023Submitted genomicNC_000003.12:g.113
    082325_113586498du
    p
    GRCh38 (hg38)NC_000003.12Chr3113,082,325113,586,498
    nssv18668023RemappedPerfectNC_000003.11:g.112
    801172_113305345du
    p
    GRCh37.p13First PassNC_000003.11Chr3112,801,172113,305,345

    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)
    nssv186680234e-061251782
    Support Center