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nsv7018863

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,838

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 38 studies. See in: genome view    
    Submitted genomic30,269,498-30,290,335Question Mark
    Overlapping variant regions from other studies: 151 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):30,665,487-30,686,324Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7018863Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2230,269,49830,290,335
    nsv7018863RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2230,665,48730,686,324

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18651553duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18651553Submitted genomicNC_000022.11:g.302
    69498_30290335dup
    GRCh38 (hg38)NC_000022.11Chr2230,269,49830,290,335
    nssv18651553RemappedPerfectNC_000022.10:g.306
    65487_30686324dup
    GRCh37.p13First PassNC_000022.10Chr2230,665,48730,686,324

    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)
    nssv186515537e-062275724
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