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nsv7061769

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:41,525

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 698 SVs from 80 studies. See in: genome view    
    Submitted genomic23,969,660-24,011,184Question Mark
    Overlapping variant regions from other studies: 1643 SVs from 102 studies. See in: genome view    
    Remapped(Score: Pass):24,311,849-24,407,634Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061769Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2223,969,66024,011,184
    nsv7061769RemappedPassGRCh37.p13Primary AssemblySecond PassNC_000022.10Chr2224,311,84924,407,634

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18763849inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18763849Submitted genomicNC_000022.11:g.239
    69660_24011184inv
    GRCh38 (hg38)NC_000022.11Chr2223,969,66024,011,184
    nssv18763849RemappedPassNC_000022.10:g.243
    11849_24407634inv
    GRCh37.p13Second PassNC_000022.10Chr2224,311,84924,407,634

    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)
    nssv187638494e-061276266
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