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nsv6866233

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 80 SVs from 23 studies. See in: genome view    
    Submitted genomic122,175,801-122,180,600Question Mark
    Overlapping variant regions from other studies: 80 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):124,938,080-124,942,879Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6866233Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9122,175,801122,180,600
    nsv6866233RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9124,938,080124,942,879

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18747381duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18747381Submitted genomicNC_000009.12:g.122
    175801_122180600du
    p
    GRCh38 (hg38)NC_000009.12Chr9122,175,801122,180,600
    nssv18747381RemappedPerfectNC_000009.11:g.124
    938080_124942879du
    p
    GRCh37.p13First PassNC_000009.11Chr9124,938,080124,942,879

    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)
    nssv187473813.3e-059270274
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