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nsv6659418

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,789

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 87 SVs from 21 studies. See in: genome view    
    Submitted genomic73,104,862-73,110,650Question Mark
    Overlapping variant regions from other studies: 87 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):73,331,990-73,337,778Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6659418Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr273,104,86273,110,650
    nsv6659418RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr273,331,99073,337,778

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18664851duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18664851Submitted genomicNC_000002.12:g.731
    04862_73110650dup
    GRCh38 (hg38)NC_000002.12Chr273,104,86273,110,650
    nssv18664851RemappedPerfectNC_000002.11:g.733
    31990_73337778dup
    GRCh37.p13First PassNC_000002.11Chr273,331,99073,337,778

    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)
    nssv186648512.9e-058274268
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