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nsv7027511

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:502,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 936 SVs from 70 studies. See in: genome view    
    Submitted genomic21,460,501-21,962,500Question Mark
    Overlapping variant regions from other studies: 936 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):21,441,139-21,943,138Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7027511Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2021,460,50121,962,500
    nsv7027511RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2021,441,13921,943,138

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18640759duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18640759Submitted genomicNC_000020.11:g.214
    60501_21962500dup
    GRCh38 (hg38)NC_000020.11Chr2021,460,50121,962,500
    nssv18640759RemappedPerfectNC_000020.10:g.214
    41139_21943138dup
    GRCh37.p13First PassNC_000020.10Chr2021,441,13921,943,138

    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)
    nssv186407594e-061273700
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