U.S. flag

An official website of the United States government

nsv6946173

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:243

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 18 studies. See in: genome view    
    Submitted genomic36,178,821-36,179,063Question Mark
    Overlapping variant regions from other studies: 104 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):36,752,958-36,753,200Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6946173Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1336,178,82136,179,063
    nsv6946173RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1336,752,95836,753,200

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18602235duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18602235Submitted genomicNC_000013.11:g.361
    78821_36179063dup
    GRCh38 (hg38)NC_000013.11Chr1336,178,82136,179,063
    nssv18602235RemappedPerfectNC_000013.10:g.367
    52958_36753200dup
    GRCh37.p13First PassNC_000013.10Chr1336,752,95836,753,200

    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)
    nssv186022352.9e-057239528
    Support Center