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nsv7040381

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,738

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 27 studies. See in: genome view    
    Submitted genomic133,347,698-133,352,435Question Mark
    Overlapping variant regions from other studies: 104 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):132,683,390-132,688,127Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7040381Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5133,347,698133,352,435
    nsv7040381RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5132,683,390132,688,127

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775340inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775340Submitted genomicNC_000005.10:g.133
    347698_133352435in
    v
    GRCh38 (hg38)NC_000005.10Chr5133,347,698133,352,435
    nssv18775340RemappedPerfectNC_000005.9:g.1326
    83390_132688127inv
    GRCh37.p13First PassNC_000005.9Chr5132,683,390132,688,127

    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)
    nssv18775340<0.00136273732
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