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nsv7064075

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,842,175

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 20918 SVs from 117 studies. See in: genome view    
    Submitted genomic49,009,324-55,851,498Question Mark
    Overlapping variant regions from other studies: 20876 SVs from 117 studies. See in: genome view    
    Remapped(Score: Good):47,625,861-54,426,554Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064075Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2049,009,32455,851,498
    nsv7064075RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2047,625,86154,426,554

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761807inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761807Submitted genomicNC_000020.11:g.490
    09324_55851498inv
    GRCh38 (hg38)NC_000020.11Chr2049,009,32455,851,498
    nssv18761807RemappedGoodNC_000020.10:g.476
    25861_54426554inv
    GRCh37.p13First PassNC_000020.10Chr2047,625,86154,426,554

    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)
    nssv187618074e-061276268
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