U.S. flag

An official website of the United States government

nsv7086123

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 289 SVs from 18 studies. See in: genome view    
    Submitted genomic19,980,701-19,990,700Question Mark
    Overlapping variant regions from other studies: 290 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):19,998,819-20,008,818Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7086123Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX19,980,70119,990,700
    nsv7086123RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX19,998,81920,008,818

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655117duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655117Submitted genomicNC_000023.11:g.199
    80701_19990700dup
    GRCh38 (hg38)NC_000023.11ChrX19,980,70119,990,700
    nssv18655117RemappedPerfectNC_000023.10:g.199
    98819_20008818dup
    GRCh37.p13First PassNC_000023.10ChrX19,998,81920,008,818

    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)
    nssv186551175e-061200000
    Support Center