U.S. flag

An official website of the United States government

nsv6583546

  • 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: 2727 SVs from 92 studies. See in: genome view    
    Submitted genomic105,350,509-106,541,811Question Mark
    Overlapping variant regions from other studies: 2729 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):105,221,236-106,412,538Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6583546Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11105,350,509106,541,811
    nsv6583546RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11105,221,236106,412,538

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18231292inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18231292Submitted genomicNC_000011.10:g.105
    350509_106541811in
    v
    GRCh38 (hg38)NC_000011.10Chr11105,350,509106,541,811
    nssv18231292RemappedPerfectNC_000011.9:g.1052
    21236_106412538inv
    GRCh37.p13First PassNC_000011.9Chr11105,221,236106,412,538

    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)
    nssv18231292<0.001139304
    Support Center