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nsv6541943

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:777,216

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2215 SVs from 94 studies. See in: genome view    
    Submitted genomic108,336,670-109,113,885Question Mark
    Overlapping variant regions from other studies: 2215 SVs from 94 studies. See in: genome view    
    Remapped(Score: Perfect):108,953,126-109,730,341Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6541943Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2108,336,670109,113,885
    nsv6541943RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2108,953,126109,730,341

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18256448inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18256448Submitted genomicNC_000002.12:g.108
    336670_109113885in
    v
    GRCh38 (hg38)NC_000002.12Chr2108,336,670109,113,885
    nssv18256448RemappedPerfectNC_000002.11:g.108
    953126_109730341in
    v
    GRCh37.p13First PassNC_000002.11Chr2108,953,126109,730,341

    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)
    nssv18256448<0.001932296
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