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nsv6852898

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:284,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1057 SVs from 68 studies. See in: genome view    
    Submitted genomic22,279,801-22,564,100Question Mark
    Overlapping variant regions from other studies: 1057 SVs from 68 studies. See in: genome view    
    Remapped(Score: Perfect):22,137,314-22,421,613Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6852898Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr822,279,80122,564,100
    nsv6852898RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr822,137,31422,421,613

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18744819duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18744819Submitted genomicNC_000008.11:g.222
    79801_22564100dup
    GRCh38 (hg38)NC_000008.11Chr822,279,80122,564,100
    nssv18744819RemappedPerfectNC_000008.10:g.221
    37314_22421613dup
    GRCh37.p13First PassNC_000008.10Chr822,137,31422,421,613

    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)
    nssv187448197e-062275440
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