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nsv7028283

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:133,029

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 517 SVs from 59 studies. See in: genome view    
    Submitted genomic38,427,807-38,560,835Question Mark
    Overlapping variant regions from other studies: 517 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):37,056,450-37,189,478Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7028283Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2038,427,80738,560,835
    nsv7028283RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2037,056,45037,189,478

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18644312duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18644312Submitted genomicNC_000020.11:g.384
    27807_38560835dup
    GRCh38 (hg38)NC_000020.11Chr2038,427,80738,560,835
    nssv18644312RemappedPerfectNC_000020.10:g.370
    56450_37189478dup
    GRCh37.p13First PassNC_000020.10Chr2037,056,45037,189,478

    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)
    nssv186443121.1e-053272320
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