U.S. flag

An official website of the United States government

nsv6519821

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,951

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 184 SVs from 22 studies. See in: genome view    
    Submitted genomic31,129,194-31,137,144Question Mark
    Overlapping variant regions from other studies: 184 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):28,709,157-28,717,107Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6519821Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1831,129,19431,137,144
    nsv6519821RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1828,709,15728,717,107

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18039894deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18039894Submitted genomicNC_000018.10:g.311
    29194_31137144del
    GRCh38 (hg38)NC_000018.10Chr1831,129,19431,137,144
    nssv18039894RemappedPerfectNC_000018.9:g.2870
    9157_28717107del
    GRCh37.p13First PassNC_000018.9Chr1828,709,15728,717,107

    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)
    nssv18039894<0.001139070
    Support Center