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nsv6920316

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:182

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 141 SVs from 29 studies. See in: genome view    
    Submitted genomic21,652,653-21,652,834Question Mark
    Overlapping variant regions from other studies: 141 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):21,805,587-21,805,768Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6920316Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1221,652,65321,652,834
    nsv6920316RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1221,805,58721,805,768

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18595728duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18595728Submitted genomicNC_000012.12:g.216
    52653_21652834dup
    GRCh38 (hg38)NC_000012.12Chr1221,652,65321,652,834
    nssv18595728RemappedPerfectNC_000012.11:g.218
    05587_21805768dup
    GRCh37.p13First PassNC_000012.11Chr1221,805,58721,805,768

    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)
    nssv185957280.002480224532
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