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nsv7033250

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:900,879

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4520 SVs from 95 studies. See in: genome view    
    Submitted genomic61,090,196-61,991,074Question Mark
    Overlapping variant regions from other studies: 4523 SVs from 95 studies. See in: genome view    
    Remapped(Score: Perfect):59,665,252-60,566,130Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7033250Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2061,090,19661,991,074
    nsv7033250RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2059,665,25260,566,130

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18645253duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18645253Submitted genomicNC_000020.11:g.610
    90196_61991074dup
    GRCh38 (hg38)NC_000020.11Chr2061,090,19661,991,074
    nssv18645253RemappedPerfectNC_000020.10:g.596
    65252_60566130dup
    GRCh37.p13First PassNC_000020.10Chr2059,665,25260,566,130

    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)
    nssv186452534e-061274912
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