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nsv7050082

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,842,286

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3942 SVs from 90 studies. See in: genome view    
    Submitted genomic154,880,025-156,722,310Question Mark
    Overlapping variant regions from other studies: 3942 SVs from 90 studies. See in: genome view    
    Remapped(Score: Perfect):155,736,537-157,578,822Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7050082Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2154,880,025156,722,310
    nsv7050082RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2155,736,537157,578,822

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18766004inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18766004Submitted genomicNC_000002.12:g.154
    880025_156722310in
    v
    GRCh38 (hg38)NC_000002.12Chr2154,880,025156,722,310
    nssv18766004RemappedPerfectNC_000002.11:g.155
    736537_157578822in
    v
    GRCh37.p13First PassNC_000002.11Chr2155,736,537157,578,822

    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)
    nssv187660045e-0514274788
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