U.S. flag

An official website of the United States government

nsv7053883

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,231,159

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2556 SVs from 101 studies. See in: genome view    
    Submitted genomic97,357,330-98,588,488Question Mark
    Overlapping variant regions from other studies: 2475 SVs from 99 studies. See in: genome view    
    Remapped(Score: Pass):98,087,758-99,204,951Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053883Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr297,357,33098,588,488
    nsv7053883RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr298,087,75899,204,951

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18770075inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18770075Submitted genomicNC_000002.12:g.973
    57330_98588488inv
    GRCh38 (hg38)NC_000002.12Chr297,357,33098,588,488
    nssv18770075RemappedPassNC_000002.11:g.980
    87758_99204951inv
    GRCh37.p13First PassNC_000002.11Chr298,087,75899,204,951

    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)
    nssv187700754e-061276268
    Support Center