U.S. flag

An official website of the United States government

nsv7046157

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,906

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 35 studies. See in: genome view    
    Submitted genomic20,692,892-20,703,797Question Mark
    Overlapping variant regions from other studies: 115 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):21,019,385-21,030,290Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7046157Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr120,692,89220,703,797
    nsv7046157RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr121,019,38521,030,290

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18738304inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18738304Submitted genomicNC_000001.11:g.206
    92892_20703797inv
    GRCh38 (hg38)NC_000001.11Chr120,692,89220,703,797
    nssv18738304RemappedPerfectNC_000001.10:g.210
    19385_21030290inv
    GRCh37.p13First PassNC_000001.10Chr121,019,38521,030,290

    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)
    nssv187383044e-061276268
    Support Center