U.S. flag

An official website of the United States government

nsv7084104

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 266 SVs from 24 studies. See in: genome view    
    Submitted genomic134,446,901-134,461,100Question Mark
    Overlapping variant regions from other studies: 266 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):133,580,931-133,595,130Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7084104Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX134,446,901134,461,100
    nsv7084104RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX133,580,931133,595,130

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655412duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655412Submitted genomicNC_000023.11:g.134
    446901_134461100du
    p
    GRCh38 (hg38)NC_000023.11ChrX134,446,901134,461,100
    nssv18655412RemappedPerfectNC_000023.10:g.133
    580931_133595130du
    p
    GRCh37.p13First PassNC_000023.10ChrX133,580,931133,595,130

    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)
    nssv186554121.4e-053214286
    Support Center