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nsv7039673

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,998,071

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 14384 SVs from 123 studies. See in: genome view    
    Submitted genomic59,959,184-65,957,254Question Mark
    Overlapping variant regions from other studies: 14401 SVs from 123 studies. See in: genome view    
    Remapped(Score: Good):59,944,910-65,942,929Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039673Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr359,959,18465,957,254
    nsv7039673RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr359,944,91065,942,929

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772377inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772377Submitted genomicNC_000003.12:g.599
    59184_65957254inv
    GRCh38 (hg38)NC_000003.12Chr359,959,18465,957,254
    nssv18772377RemappedGoodNC_000003.11:g.599
    44910_65942929inv
    GRCh37.p13First PassNC_000003.11Chr359,944,91065,942,929

    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)
    nssv187723771.1e-053272640
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