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nsv7043397

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,757

    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 genomic163,317,150-163,318,906Question Mark
    Overlapping variant regions from other studies: 108 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):163,286,940-163,288,696Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043397Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1163,317,150163,318,906
    nsv7043397RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1163,286,940163,288,696

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18746878inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18746878Submitted genomicNC_000001.11:g.163
    317150_163318906in
    v
    GRCh38 (hg38)NC_000001.11Chr1163,317,150163,318,906
    nssv18746878RemappedPerfectNC_000001.10:g.163
    286940_163288696in
    v
    GRCh37.p13First PassNC_000001.10Chr1163,286,940163,288,696

    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)
    nssv187468784e-061276268
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