U.S. flag

An official website of the United States government

nsv7091326

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:286,436

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 597 SVs from 54 studies. See in: genome view    
    Submitted genomic26,067,986-26,354,421Question Mark
    Overlapping variant regions from other studies: 598 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):26,086,103-26,372,538Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7091326Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX26,067,98626,354,421
    nsv7091326RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX26,086,10326,372,538

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655285duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655285Submitted genomicNC_000023.11:g.260
    67986_26354421dup
    GRCh38 (hg38)NC_000023.11ChrX26,067,98626,354,421
    nssv18655285RemappedPerfectNC_000023.10:g.260
    86103_26372538dup
    GRCh37.p13First PassNC_000023.10ChrX26,086,10326,372,538

    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)
    nssv186552855e-061200000
    Support Center