U.S. flag

An official website of the United States government

nsv7053451

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 131 SVs from 25 studies. See in: genome view    
    Submitted genomic142,332,262-142,332,289Question Mark
    Overlapping variant regions from other studies: 131 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):143,253,415-143,253,442Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053451Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4142,332,262142,332,289
    nsv7053451RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4143,253,415143,253,442

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18771988inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18771988Submitted genomicNC_000004.12:g.142
    332262_142332289in
    v
    GRCh38 (hg38)NC_000004.12Chr4142,332,262142,332,289
    nssv18771988RemappedPerfectNC_000004.11:g.143
    253415_143253442in
    v
    GRCh37.p13First PassNC_000004.11Chr4143,253,415143,253,442

    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)
    nssv18771988<0.001154273906
    Support Center