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nsv7011299

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 308 SVs from 47 studies. See in: genome view    
    Submitted genomic5,048,501-5,105,700Question Mark
    Overlapping variant regions from other studies: 308 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):5,029,147-5,086,346Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7011299Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr205,048,5015,105,700
    nsv7011299RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr205,029,1475,086,346

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18645040duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18645040Submitted genomicNC_000020.11:g.504
    8501_5105700dup
    GRCh38 (hg38)NC_000020.11Chr205,048,5015,105,700
    nssv18645040RemappedPerfectNC_000020.10:g.502
    9147_5086346dup
    GRCh37.p13First PassNC_000020.10Chr205,029,1475,086,346

    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)
    nssv186450402.1e-056275748
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