U.S. flag

An official website of the United States government

nsv7039200

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:167,155

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 420 SVs from 64 studies. See in: genome view    
    Submitted genomic43,310,824-43,477,978Question Mark
    Overlapping variant regions from other studies: 420 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):43,776,495-43,943,649Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039200Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr143,310,82443,477,978
    nsv7039200RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr143,776,49543,943,649

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760991inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760991Submitted genomicNC_000001.11:g.433
    10824_43477978inv
    GRCh38 (hg38)NC_000001.11Chr143,310,82443,477,978
    nssv18760991RemappedPerfectNC_000001.10:g.437
    76495_43943649inv
    GRCh37.p13First PassNC_000001.10Chr143,776,49543,943,649

    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)
    nssv187609914e-061276268
    Support Center