U.S. flag

An official website of the United States government

nsv7066985

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:694,625

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1122 SVs from 57 studies. See in: genome view    
    Submitted genomic12,854,465-13,549,089Question Mark
    Overlapping variant regions from other studies: 1123 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):12,872,584-13,567,208Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066985Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX12,854,46513,549,089
    nsv7066985RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX12,872,58413,567,208

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655053duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655053Submitted genomicNC_000023.11:g.128
    54465_13549089dup
    GRCh38 (hg38)NC_000023.11ChrX12,854,46513,549,089
    nssv18655053RemappedPerfectNC_000023.10:g.128
    72584_13567208dup
    GRCh37.p13First PassNC_000023.10ChrX12,872,58413,567,208

    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)
    nssv186550535e-061200000
    Support Center