U.S. flag

An official website of the United States government

nsv7062969

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,699

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 102 SVs from 15 studies. See in: genome view    
    Submitted genomic48,668,170-48,672,868Question Mark
    Overlapping variant regions from other studies: 102 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):47,284,708-47,289,406Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7062969Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2048,668,17048,672,868
    nsv7062969RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2047,284,70847,289,406

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761800inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761800Submitted genomicNC_000020.11:g.486
    68170_48672868inv
    GRCh38 (hg38)NC_000020.11Chr2048,668,17048,672,868
    nssv18761800RemappedPerfectNC_000020.10:g.472
    84708_47289406inv
    GRCh37.p13First PassNC_000020.10Chr2047,284,70847,289,406

    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)
    nssv187618004e-061276268
    Support Center