U.S. flag

An official website of the United States government

nsv7067025

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:889,229

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2466 SVs from 88 studies. See in: genome view    
    Submitted genomic22,307,930-23,197,158Question Mark
    Overlapping variant regions from other studies: 2466 SVs from 88 studies. See in: genome view    
    Remapped(Score: Perfect):22,329,476-23,218,704Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067025Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1122,307,93023,197,158
    nsv7067025RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1122,329,47623,218,704

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18738114inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18738114Submitted genomicNC_000011.10:g.223
    07930_23197158inv
    GRCh38 (hg38)NC_000011.10Chr1122,307,93023,197,158
    nssv18738114RemappedPerfectNC_000011.9:g.2232
    9476_23218704inv
    GRCh37.p13First PassNC_000011.9Chr1122,329,47623,218,704

    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)
    nssv187381144e-061276258
    Support Center