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nsv6549694

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,169,913

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7307 SVs from 101 studies. See in: genome view    
    Submitted genomic155,298,173-158,468,085Question Mark
    Overlapping variant regions from other studies: 7314 SVs from 101 studies. See in: genome view    
    Remapped(Score: Perfect):155,267,964-158,437,875Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6549694Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1155,298,173158,468,085
    nsv6549694RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1155,267,964158,437,875

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18247108inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18247108Submitted genomicNC_000001.11:g.155
    298173_158468085in
    v
    GRCh38 (hg38)NC_000001.11Chr1155,298,173158,468,085
    nssv18247108RemappedPerfectNC_000001.10:g.155
    267964_158437875in
    v
    GRCh37.p13First PassNC_000001.10Chr1155,267,964158,437,875

    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)
    nssv18247108<0.001139304
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