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nsv7070079

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:47,730

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 257 SVs from 35 studies. See in: genome view    
    Submitted genomic49,023,937-49,071,666Question Mark
    Overlapping variant regions from other studies: 255 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):47,101,299-47,149,028Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070079Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1749,023,93749,071,666
    nsv7070079RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1747,101,29947,149,028

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758966inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758966Submitted genomicNC_000017.11:g.490
    23937_49071666inv
    GRCh38 (hg38)NC_000017.11Chr1749,023,93749,071,666
    nssv18758966RemappedPerfectNC_000017.10:g.471
    01299_47149028inv
    GRCh37.p13First PassNC_000017.10Chr1747,101,29947,149,028

    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)
    nssv187589662.2e-056272316
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