U.S. flag

An official website of the United States government

nsv7063109

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,946

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 235 SVs from 26 studies. See in: genome view    
    Submitted genomic14,407,583-14,409,528Question Mark
    Overlapping variant regions from other studies: 241 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):14,407,581-14,409,526Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063109Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr914,407,58314,409,528
    nsv7063109RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr914,407,58114,409,526

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785712inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785712Submitted genomicNC_000009.12:g.144
    07583_14409528inv
    GRCh38 (hg38)NC_000009.12Chr914,407,58314,409,528
    nssv18785712RemappedPerfectNC_000009.11:g.144
    07581_14409526inv
    GRCh37.p13First PassNC_000009.11Chr914,407,58114,409,526

    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)
    nssv187857127e-062274908
    Support Center