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nsv6903029

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86,123

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 298 SVs from 41 studies. See in: genome view    
    Submitted genomic46,727,780-46,813,902Question Mark
    Overlapping variant regions from other studies: 298 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):46,749,330-46,835,452Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6903029Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1146,727,78046,813,902
    nsv6903029RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1146,749,33046,835,452

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18579703duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18579703Submitted genomicNC_000011.10:g.467
    27780_46813902dup
    GRCh38 (hg38)NC_000011.10Chr1146,727,78046,813,902
    nssv18579703RemappedPerfectNC_000011.9:g.4674
    9330_46835452dup
    GRCh37.p13First PassNC_000011.9Chr1146,749,33046,835,452

    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)
    nssv185797037e-062275836
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