U.S. flag

An official website of the United States government

nsv6975318

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,809

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 182 SVs from 33 studies. See in: genome view    
    Submitted genomic3,675,081-3,682,889Question Mark
    Overlapping variant regions from other studies: 182 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):3,725,082-3,732,890Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6975318Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr163,675,0813,682,889
    nsv6975318RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr163,725,0823,732,890

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18401940deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18401940Submitted genomicNC_000016.10:g.367
    5081_3682889del
    GRCh38 (hg38)NC_000016.10Chr163,675,0813,682,889
    nssv18401940RemappedPerfectNC_000016.9:g.3725
    082_3732890del
    GRCh37.p13First PassNC_000016.9Chr163,725,0823,732,890

    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)
    nssv184019401.4e-054276228
    Support Center