U.S. flag

An official website of the United States government

nsv6904589

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,771

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 69 SVs from 24 studies. See in: genome view    
    Submitted genomic6,107,420-6,113,190Question Mark
    Overlapping variant regions from other studies: 69 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):6,128,650-6,134,420Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6904589Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr116,107,4206,113,190
    nsv6904589RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr116,128,6506,134,420

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18583417duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18583417Submitted genomicNC_000011.10:g.610
    7420_6113190dup
    GRCh38 (hg38)NC_000011.10Chr116,107,4206,113,190
    nssv18583417RemappedPerfectNC_000011.9:g.6128
    650_6134420dup
    GRCh37.p13First PassNC_000011.9Chr116,128,6506,134,420

    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)
    nssv185834174e-061273842
    Support Center