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nsv7064311

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:553,048

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1899 SVs from 90 studies. See in: genome view    
    Submitted genomic99,320,520-99,873,567Question Mark
    Overlapping variant regions from other studies: 1899 SVs from 90 studies. See in: genome view    
    Remapped(Score: Perfect):99,860,725-100,413,772Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064311Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1599,320,52099,873,567
    nsv7064311RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1599,860,725100,413,772

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756766inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756766Submitted genomicNC_000015.10:g.993
    20520_99873567inv
    GRCh38 (hg38)NC_000015.10Chr1599,320,52099,873,567
    nssv18756766RemappedPerfectNC_000015.9:g.9986
    0725_100413772inv
    GRCh37.p13First PassNC_000015.9Chr1599,860,725100,413,772

    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)
    nssv187567667e-062274978
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