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nsv7060184

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,980,786

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8074 SVs from 109 studies. See in: genome view    
    Submitted genomic13,148,010-16,128,795Question Mark
    Overlapping variant regions from other studies: 8074 SVs from 109 studies. See in: genome view    
    Remapped(Score: Perfect):13,190,010-16,170,794Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060184Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1013,148,01016,128,795
    nsv7060184RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1013,190,01016,170,794

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18731879inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18731879Submitted genomicNC_000010.11:g.131
    48010_16128795inv
    GRCh38 (hg38)NC_000010.11Chr1013,148,01016,128,795
    nssv18731879RemappedPerfectNC_000010.10:g.131
    90010_16170794inv
    GRCh37.p13First PassNC_000010.10Chr1013,190,01016,170,794

    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)
    nssv187318794e-061276268
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