U.S. flag

An official website of the United States government

nsv6414436

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:482

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 20 studies. See in: genome view    
    Submitted genomic44,168,359-44,168,840Question Mark
    Overlapping variant regions from other studies: 99 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):44,136,096-44,136,577Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6414436Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr644,168,35944,168,840
    nsv6414436RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr644,136,09644,136,577

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18226641duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18226641Submitted genomicNC_000006.12:g.441
    68359_44168840dup
    GRCh38 (hg38)NC_000006.12Chr644,168,35944,168,840
    nssv18226641RemappedPerfectNC_000006.11:g.441
    36096_44136577dup
    GRCh37.p13First PassNC_000006.11Chr644,136,09644,136,577

    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)
    nssv18226641<0.001537706
    Support Center