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nsv7055882

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:189,738

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 435 SVs from 55 studies. See in: genome view    
    Submitted genomic120,635,987-120,825,724Question Mark
    Overlapping variant regions from other studies: 435 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):120,276,041-120,465,778Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055882Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7120,635,987120,825,724
    nsv7055882RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7120,276,041120,465,778

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18780029inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18780029Submitted genomicNC_000007.14:g.120
    635987_120825724in
    v
    GRCh38 (hg38)NC_000007.14Chr7120,635,987120,825,724
    nssv18780029RemappedPerfectNC_000007.13:g.120
    276041_120465778in
    v
    GRCh37.p13First PassNC_000007.13Chr7120,276,041120,465,778

    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)
    nssv187800294e-061276268
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