U.S. flag

An official website of the United States government

nsv7086239

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 271 SVs from 17 studies. See in: genome view    
    Submitted genomic24,173,601-24,178,900Question Mark
    Overlapping variant regions from other studies: 272 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):24,191,718-24,197,017Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7086239Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX24,173,60124,178,900
    nsv7086239RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX24,191,71824,197,017

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655210duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655210Submitted genomicNC_000023.11:g.241
    73601_24178900dup
    GRCh38 (hg38)NC_000023.11ChrX24,173,60124,178,900
    nssv18655210RemappedPerfectNC_000023.10:g.241
    91718_24197017dup
    GRCh37.p13First PassNC_000023.10ChrX24,191,71824,197,017

    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)
    nssv186552105e-061200000
    Support Center