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nsv6893948

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 87 SVs from 16 studies. See in: genome view    
    Submitted genomic110,286,801-110,289,400Question Mark
    Overlapping variant regions from other studies: 87 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):112,046,559-112,049,158Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6893948Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10110,286,801110,289,400
    nsv6893948RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10112,046,559112,049,158

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18586650duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18586650Submitted genomicNC_000010.11:g.110
    286801_110289400du
    p
    GRCh38 (hg38)NC_000010.11Chr10110,286,801110,289,400
    nssv18586650RemappedPerfectNC_000010.10:g.112
    046559_112049158du
    p
    GRCh37.p13First PassNC_000010.10Chr10112,046,559112,049,158

    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)
    nssv185866504e-061273296
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