U.S. flag

An official website of the United States government

nsv7046422

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,033,398

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4104 SVs from 106 studies. See in: genome view    
    Submitted genomic245,013,208-246,046,605Question Mark
    Overlapping variant regions from other studies: 4107 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):245,176,510-246,209,907Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7046422Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1245,013,208246,046,605
    nsv7046422RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1245,176,510246,209,907

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759459inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759459Submitted genomicNC_000001.11:g.245
    013208_246046605in
    v
    GRCh38 (hg38)NC_000001.11Chr1245,013,208246,046,605
    nssv18759459RemappedPerfectNC_000001.10:g.245
    176510_246209907in
    v
    GRCh37.p13First PassNC_000001.10Chr1245,176,510246,209,907

    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)
    nssv187594591.1e-053274452
    Support Center