U.S. flag

An official website of the United States government

nsv6902273

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,395

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 123 SVs from 30 studies. See in: genome view    
    Submitted genomic46,607,086-46,610,480Question Mark
    Overlapping variant regions from other studies: 123 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):46,628,636-46,632,030Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6902273Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1146,607,08646,610,480
    nsv6902273RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1146,628,63646,632,030

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18582487duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18582487Submitted genomicNC_000011.10:g.466
    07086_46610480dup
    GRCh38 (hg38)NC_000011.10Chr1146,607,08646,610,480
    nssv18582487RemappedPerfectNC_000011.9:g.4662
    8636_46632030dup
    GRCh37.p13First PassNC_000011.9Chr1146,628,63646,632,030

    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)
    nssv18582487<0.00186274180
    Support Center