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nsv6578547

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,950,474

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 15273 SVs from 123 studies. See in: genome view    
    Submitted genomic104,070,004-110,020,477Question Mark
    Overlapping variant regions from other studies: 15276 SVs from 123 studies. See in: genome view    
    Remapped(Score: Perfect):103,940,732-109,891,203Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6578547Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11104,070,004110,020,477
    nsv6578547RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11103,940,732109,891,203

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18221435inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18221435Submitted genomicNC_000011.10:g.104
    070004_110020477in
    v
    GRCh38 (hg38)NC_000011.10Chr11104,070,004110,020,477
    nssv18221435RemappedPerfectNC_000011.9:g.1039
    40732_109891203inv
    GRCh37.p13First PassNC_000011.9Chr11103,940,732109,891,203

    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)
    nssv18221435<0.001139304
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