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nsv7058604

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,332

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 34 studies. See in: genome view    
    Submitted genomic116,162,480-116,173,811Question Mark
    Overlapping variant regions from other studies: 118 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):117,921,992-117,933,323Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058604Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10116,162,480116,173,811
    nsv7058604RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10117,921,992117,933,323

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18732152inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18732152Submitted genomicNC_000010.11:g.116
    162480_116173811in
    v
    GRCh38 (hg38)NC_000010.11Chr10116,162,480116,173,811
    nssv18732152RemappedPerfectNC_000010.10:g.117
    921992_117933323in
    v
    GRCh37.p13First PassNC_000010.10Chr10117,921,992117,933,323

    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)
    nssv187321529.6e-0527274012
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