U.S. flag

An official website of the United States government

nsv7068132

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,948,902

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6076 SVs from 104 studies. See in: genome view    
    Submitted genomic23,065,120-25,014,021Question Mark
    Overlapping variant regions from other studies: 6076 SVs from 104 studies. See in: genome view    
    Remapped(Score: Perfect):23,639,259-25,588,159Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068132Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1323,065,12025,014,021
    nsv7068132RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1323,639,25925,588,159

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752880inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752880Submitted genomicNC_000013.11:g.230
    65120_25014021inv
    GRCh38 (hg38)NC_000013.11Chr1323,065,12025,014,021
    nssv18752880RemappedPerfectNC_000013.10:g.236
    39259_25588159inv
    GRCh37.p13First PassNC_000013.10Chr1323,639,25925,588,159

    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)
    nssv187528801.4e-054272982
    Support Center