nsv7083957

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,733

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 253 SVs from 23 studies. See in: genome view    
    Submitted genomic132,810,368-132,814,100Question Mark
    Overlapping variant regions from other studies: 253 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):131,944,396-131,948,128Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7083957Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX132,810,368132,814,100
    nsv7083957RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX131,944,396131,948,128

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18653697duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18653697Submitted genomicNC_000023.11:g.132
    810368_132814100du
    p
    GRCh38 (hg38)NC_000023.11ChrX132,810,368132,814,100
    nssv18653697RemappedPerfectNC_000023.10:g.131
    944396_131948128du
    p
    GRCh37.p13First PassNC_000023.10ChrX131,944,396131,948,128

    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)
    nssv186536975e-061200000
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