U.S. flag

An official website of the United States government

nsv7019948

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,412,236

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 11982 SVs from 115 studies. See in: genome view    
    Submitted genomic40,558,832-43,971,067Question Mark
    Overlapping variant regions from other studies: 12002 SVs from 115 studies. See in: genome view    
    Remapped(Score: Good):41,930,759-45,390,948Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7019948Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2140,558,83243,971,067
    nsv7019948RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2141,930,75945,390,948

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18644019duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18644019Submitted genomicNC_000021.9:g.4055
    8832_43971067dup
    GRCh38 (hg38)NC_000021.9Chr2140,558,83243,971,067
    nssv18644019RemappedGoodNC_000021.8:g.4193
    0759_45390948dup
    GRCh37.p13First PassNC_000021.8Chr2141,930,75945,390,948

    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)
    nssv186440197e-062275814
    Support Center