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nsv7034106

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:108,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 661 SVs from 71 studies. See in: genome view    
    Submitted genomic62,767,501-62,875,500Question Mark
    Overlapping variant regions from other studies: 661 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):61,398,853-61,506,852Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7034106Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2062,767,50162,875,500
    nsv7034106RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2061,398,85361,506,852

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18643025duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18643025Submitted genomicNC_000020.11:g.627
    67501_62875500dup
    GRCh38 (hg38)NC_000020.11Chr2062,767,50162,875,500
    nssv18643025RemappedPerfectNC_000020.10:g.613
    98853_61506852dup
    GRCh37.p13First PassNC_000020.10Chr2061,398,85361,506,852

    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)
    nssv186430251.8e-053159336
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