U.S. flag

An official website of the United States government

nsv7030082

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,419

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 200 SVs from 38 studies. See in: genome view    
    Submitted genomic63,291,998-63,297,416Question Mark
    Overlapping variant regions from other studies: 200 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):61,923,350-61,928,768Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7030082Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2063,291,99863,297,416
    nsv7030082RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2061,923,35061,928,768

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18435548deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18435548Submitted genomicNC_000020.11:g.632
    91998_63297416del
    GRCh38 (hg38)NC_000020.11Chr2063,291,99863,297,416
    nssv18435548RemappedPerfectNC_000020.10:g.619
    23350_61928768del
    GRCh37.p13First PassNC_000020.10Chr2061,923,35061,928,768

    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)
    nssv184355481.1e-053275550
    Support Center