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nsv7012902

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:251,366

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1127 SVs from 75 studies. See in: genome view    
    Submitted genomic5,466,465-5,717,830Question Mark
    Overlapping variant regions from other studies: 1127 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):5,447,111-5,698,476Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7012902Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr205,466,4655,717,830
    nsv7012902RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr205,447,1115,698,476

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18644401duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18644401Submitted genomicNC_000020.11:g.546
    6465_5717830dup
    GRCh38 (hg38)NC_000020.11Chr205,466,4655,717,830
    nssv18644401RemappedPerfectNC_000020.10:g.544
    7111_5698476dup
    GRCh37.p13First PassNC_000020.10Chr205,447,1115,698,476

    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)
    nssv186444017e-062275530
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