U.S. flag

An official website of the United States government

nsv7059173

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,216,440

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9053 SVs from 105 studies. See in: genome view    
    Submitted genomic65,003,895-68,220,334Question Mark
    Overlapping variant regions from other studies: 7986 SVs from 99 studies. See in: genome view    
    Remapped(Score: Pass):63,000,013-65,936,105Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059173Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1765,003,89568,220,334
    nsv7059173RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1763,000,01365,936,105

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759129inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759129Submitted genomicNC_000017.11:g.650
    03895_68220334inv
    GRCh38 (hg38)NC_000017.11Chr1765,003,89568,220,334
    nssv18759129RemappedPassNC_000017.10:g.630
    00013_65936105inv
    GRCh37.p13First PassNC_000017.10Chr1763,000,01365,936,105

    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)
    nssv187591290.0174350268124
    Support Center