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nsv6978904

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42,368

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 249 SVs from 44 studies. See in: genome view    
    Submitted genomic39,024,796-39,067,163Question Mark
    Overlapping variant regions from other studies: 248 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):37,181,049-37,223,416Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6978904Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1739,024,79639,067,163
    nsv6978904RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1737,181,04937,223,416

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18628694duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18628694Submitted genomicNC_000017.11:g.390
    24796_39067163dup
    GRCh38 (hg38)NC_000017.11Chr1739,024,79639,067,163
    nssv18628694RemappedPerfectNC_000017.10:g.371
    81049_37223416dup
    GRCh37.p13First PassNC_000017.10Chr1737,181,04937,223,416

    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)
    nssv186286944e-061276058
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