U.S. flag

An official website of the United States government

nsv7088507

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 326 SVs from 40 studies. See in: genome view    
    Submitted genomic69,473,301-69,559,800Question Mark
    Overlapping variant regions from other studies: 326 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):68,693,144-68,779,643Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7088507Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX69,473,30169,559,800
    nsv7088507RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX68,693,14468,779,643

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18659092duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18659092Submitted genomicNC_000023.11:g.694
    73301_69559800dup
    GRCh38 (hg38)NC_000023.11ChrX69,473,30169,559,800
    nssv18659092RemappedPerfectNC_000023.10:g.686
    93144_68779643dup
    GRCh37.p13First PassNC_000023.10ChrX68,693,14468,779,643

    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)
    nssv186590925e-061200000
    Support Center