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nsv7065344

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,162,843

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9689 SVs from 104 studies. See in: genome view    
    Submitted genomic49,128,244-52,291,086Question Mark
    Overlapping variant regions from other studies: 9692 SVs from 104 studies. See in: genome view    
    Remapped(Score: Perfect):47,744,781-50,907,625Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065344Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2049,128,24452,291,086
    nsv7065344RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2047,744,78150,907,625

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761810inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761810Submitted genomicNC_000020.11:g.491
    28244_52291086inv
    GRCh38 (hg38)NC_000020.11Chr2049,128,24452,291,086
    nssv18761810RemappedPerfectNC_000020.10:g.477
    44781_50907625inv
    GRCh37.p13First PassNC_000020.10Chr2047,744,78150,907,625

    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)
    nssv18761810<0.00145273624
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