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nsv7055117

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 73 SVs from 11 studies. See in: genome view    
    Submitted genomic149,587,148-149,587,166Question Mark
    Overlapping variant regions from other studies: 73 SVs from 11 studies. See in: genome view    
    Remapped(Score: Perfect):148,966,711-148,966,729Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055117Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5149,587,148149,587,166
    nsv7055117RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5148,966,711148,966,729

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774302inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774302Submitted genomicNC_000005.10:g.149
    587148_149587166in
    v
    GRCh38 (hg38)NC_000005.10Chr5149,587,148149,587,166
    nssv18774302RemappedPerfectNC_000005.9:g.1489
    66711_148966729inv
    GRCh37.p13First PassNC_000005.9Chr5148,966,711148,966,729

    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)
    nssv187743020.001301274388
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