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nsv6992930

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24,736

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 235 SVs from 41 studies. See in: genome view    
    Submitted genomic72,889,166-72,913,901Question Mark
    Overlapping variant regions from other studies: 235 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):70,885,305-70,910,040Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6992930Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1772,889,16672,913,901
    nsv6992930RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1770,885,30570,910,040

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18628562duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18628562Submitted genomicNC_000017.11:g.728
    89166_72913901dup
    GRCh38 (hg38)NC_000017.11Chr1772,889,16672,913,901
    nssv18628562RemappedPerfectNC_000017.10:g.708
    85305_70910040dup
    GRCh37.p13First PassNC_000017.10Chr1770,885,30570,910,040

    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)
    nssv186285621.8e-055275692
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