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nsv7033075

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:676,026

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3809 SVs from 91 studies. See in: genome view    
    Submitted genomic49,877,724-50,553,749Question Mark
    Overlapping variant regions from other studies: 3783 SVs from 91 studies. See in: genome view    
    Remapped(Score: Pass):50,271,372-50,992,178Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7033075Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2249,877,72450,553,749
    nsv7033075RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2250,271,37250,992,178

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18654014duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18654014Submitted genomicNC_000022.11:g.498
    77724_50553749dup
    GRCh38 (hg38)NC_000022.11Chr2249,877,72450,553,749
    nssv18654014RemappedPassNC_000022.10:g.502
    71372_50992178dup
    GRCh37.p13First PassNC_000022.10Chr2250,271,37250,992,178

    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)
    nssv186540147e-062269954
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