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nsv7022309

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,615

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 216 SVs from 46 studies. See in: genome view    
    Submitted genomic61,692,678-61,722,292Question Mark
    Overlapping variant regions from other studies: 216 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):60,267,734-60,297,348Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7022309Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2061,692,67861,722,292
    nsv7022309RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2060,267,73460,297,348

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18645298duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18645298Submitted genomicNC_000020.11:g.616
    92678_61722292dup
    GRCh38 (hg38)NC_000020.11Chr2061,692,67861,722,292
    nssv18645298RemappedPerfectNC_000020.10:g.602
    67734_60297348dup
    GRCh37.p13First PassNC_000020.10Chr2060,267,73460,297,348

    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)
    nssv186452984.3e-0512275430
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