U.S. flag

An official website of the United States government

nsv6985050

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,625

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 512 SVs from 47 studies. See in: genome view    
    Submitted genomic29,967,581-29,970,205Question Mark
    Overlapping variant regions from other studies: 512 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):29,978,902-29,981,526Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6985050Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1629,967,58129,970,205
    nsv6985050RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1629,978,90229,981,526

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18398554deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18398554Submitted genomicNC_000016.10:g.299
    67581_29970205del
    GRCh38 (hg38)NC_000016.10Chr1629,967,58129,970,205
    nssv18398554RemappedPerfectNC_000016.9:g.2997
    8902_29981526del
    GRCh37.p13First PassNC_000016.9Chr1629,978,90229,981,526

    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)
    nssv183985544.3e-0512275750
    Support Center