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nsv7056812

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,037

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 27 studies. See in: genome view    
    Submitted genomic31,656,297-31,659,333Question Mark
    Overlapping variant regions from other studies: 143 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):31,624,074-31,627,110Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7056812Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr631,656,29731,659,333
    nsv7056812RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr631,624,07431,627,110

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18778587inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18778587Submitted genomicNC_000006.12:g.316
    56297_31659333inv
    GRCh38 (hg38)NC_000006.12Chr631,656,29731,659,333
    nssv18778587RemappedPerfectNC_000006.11:g.316
    24074_31627110inv
    GRCh37.p13First PassNC_000006.11Chr631,624,07431,627,110

    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)
    nssv187785874e-060276268
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