U.S. flag

An official website of the United States government

nsv6514620

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:575

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 83 SVs from 21 studies. See in: genome view    
    Submitted genomic94,192,107-94,192,681Question Mark
    Overlapping variant regions from other studies: 89 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):94,658,444-94,659,018Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6514620Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1494,192,10794,192,681
    nsv6514620RemappedPerfectGRCh37.p13Primary AssemblySecond PassNC_000014.8Chr1494,658,44494,659,018

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18022918deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18022918Submitted genomicNC_000014.9:g.9419
    2107_94192681del
    GRCh38 (hg38)NC_000014.9Chr1494,192,10794,192,681
    nssv18022918RemappedPerfectNC_000014.8:g.9465
    8444_94659018del
    GRCh37.p13Second PassNC_000014.8Chr1494,658,44494,659,018

    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)
    nssv18022918<0.001638540
    Support Center