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nsv7067005

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:617,037

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1845 SVs from 80 studies. See in: genome view    
    Submitted genomic14,123,920-14,740,956Question Mark
    Overlapping variant regions from other studies: 1846 SVs from 80 studies. See in: genome view    
    Remapped(Score: Perfect):14,276,854-14,893,890Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067005Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1214,123,92014,740,956
    nsv7067005RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1214,276,85414,893,890

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752196inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752196Submitted genomicNC_000012.12:g.141
    23920_14740956inv
    GRCh38 (hg38)NC_000012.12Chr1214,123,92014,740,956
    nssv18752196RemappedPerfectNC_000012.11:g.142
    76854_14893890inv
    GRCh37.p13First PassNC_000012.11Chr1214,276,85414,893,890

    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)
    nssv187521967e-062274748
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