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nsv6848735

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:142,296

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 482 SVs from 51 studies. See in: genome view    
    Submitted genomic67,335,815-67,478,110Question Mark
    Overlapping variant regions from other studies: 482 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):68,248,050-68,390,345Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6848735Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr867,335,81567,478,110
    nsv6848735RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr868,248,05068,390,345

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18736717duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18736717Submitted genomicNC_000008.11:g.673
    35815_67478110dup
    GRCh38 (hg38)NC_000008.11Chr867,335,81567,478,110
    nssv18736717RemappedPerfectNC_000008.10:g.682
    48050_68390345dup
    GRCh37.p13First PassNC_000008.10Chr868,248,05068,390,345

    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)
    nssv187367177e-062275102
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