U.S. flag

An official website of the United States government

nsv7063726

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,191,303

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2726 SVs from 92 studies. See in: genome view    
    Submitted genomic105,350,510-106,541,812Question Mark
    Overlapping variant regions from other studies: 2728 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):105,221,237-106,412,539Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063726Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11105,350,510106,541,812
    nsv7063726RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11105,221,237106,412,539

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18732524inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18732524Submitted genomicNC_000011.10:g.105
    350510_106541812in
    v
    GRCh38 (hg38)NC_000011.10Chr11105,350,510106,541,812
    nssv18732524RemappedPerfectNC_000011.9:g.1052
    21237_106412539inv
    GRCh37.p13First PassNC_000011.9Chr11105,221,237106,412,539

    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)
    nssv187325241.8e-055274018
    Support Center