U.S. flag

An official website of the United States government

nsv7063169

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,225

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 30 studies. See in: genome view    
    Submitted genomic21,459,547-21,471,771Question Mark
    Overlapping variant regions from other studies: 94 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):21,481,093-21,493,317Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063169Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1121,459,54721,471,771
    nsv7063169RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1121,481,09321,493,317

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18740334inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18740334Submitted genomicNC_000011.10:g.214
    59547_21471771inv
    GRCh38 (hg38)NC_000011.10Chr1121,459,54721,471,771
    nssv18740334RemappedPerfectNC_000011.9:g.2148
    1093_21493317inv
    GRCh37.p13First PassNC_000011.9Chr1121,481,09321,493,317

    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)
    nssv187403344e-061276268
    Support Center