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nsv7051442

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,720,326

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 11139 SVs from 116 studies. See in: genome view    
    Submitted genomic120,525,437-125,245,762Question Mark
    Overlapping variant regions from other studies: 11140 SVs from 116 studies. See in: genome view    
    Remapped(Score: Perfect):120,846,583-125,566,908Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051442Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6120,525,437125,245,762
    nsv7051442RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6120,846,583125,566,908

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18778791inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18778791Submitted genomicNC_000006.12:g.120
    525437_125245762in
    v
    GRCh38 (hg38)NC_000006.12Chr6120,525,437125,245,762
    nssv18778791RemappedPerfectNC_000006.11:g.120
    846583_125566908in
    v
    GRCh37.p13First PassNC_000006.11Chr6120,846,583125,566,908

    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)
    nssv187787911.1e-053273324
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