U.S. flag

An official website of the United States government

nsv7086081

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:95,843

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 411 SVs from 37 studies. See in: genome view    
    Submitted genomic19,483,433-19,579,275Question Mark
    Overlapping variant regions from other studies: 412 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):19,501,551-19,597,393Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7086081Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX19,483,43319,579,275
    nsv7086081RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX19,501,55119,597,393

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18656657duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18656657Submitted genomicNC_000023.11:g.194
    83433_19579275dup
    GRCh38 (hg38)NC_000023.11ChrX19,483,43319,579,275
    nssv18656657RemappedPerfectNC_000023.10:g.195
    01551_19597393dup
    GRCh37.p13First PassNC_000023.10ChrX19,501,55119,597,393

    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)
    nssv186566575e-061200000
    Support Center