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nsv7074141

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,966,629

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7485 SVs from 114 studies. See in: genome view    
    Submitted genomic48,828,025-51,794,653Question Mark
    Overlapping variant regions from other studies: 7485 SVs from 114 studies. See in: genome view    
    Remapped(Score: Perfect):49,740,584-52,707,213Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074141Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr848,828,02551,794,653
    nsv7074141RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr849,740,58452,707,213

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18782438inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18782438Submitted genomicNC_000008.11:g.488
    28025_51794653inv
    GRCh38 (hg38)NC_000008.11Chr848,828,02551,794,653
    nssv18782438RemappedPerfectNC_000008.10:g.497
    40584_52707213inv
    GRCh37.p13First PassNC_000008.10Chr849,740,58452,707,213

    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)
    nssv187824384e-061276268
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