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nsv6993908

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,512

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 24 studies. See in: genome view    
    Submitted genomic67,568,543-67,581,054Question Mark
    Overlapping variant regions from other studies: 134 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):65,564,659-65,577,170Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6993908Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1767,568,54367,581,054
    nsv6993908RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1765,564,65965,577,170

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18627666duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18627666Submitted genomicNC_000017.11:g.675
    68543_67581054dup
    GRCh38 (hg38)NC_000017.11Chr1767,568,54367,581,054
    nssv18627666RemappedPerfectNC_000017.10:g.655
    64659_65577170dup
    GRCh37.p13First PassNC_000017.10Chr1765,564,65965,577,170

    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)
    nssv186276664e-061276058
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