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nsv7021742

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:207,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 737 SVs from 60 studies. See in: genome view    
    Submitted genomic42,779,701-42,986,800Question Mark
    Overlapping variant regions from other studies: 737 SVs from 60 studies. See in: genome view    
    Remapped(Score: Perfect):43,175,707-43,382,806Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7021742Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2242,779,70142,986,800
    nsv7021742RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2243,175,70743,382,806

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18651611duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18651611Submitted genomicNC_000022.11:g.427
    79701_42986800dup
    GRCh38 (hg38)NC_000022.11Chr2242,779,70142,986,800
    nssv18651611RemappedPerfectNC_000022.10:g.431
    75707_43382806dup
    GRCh37.p13First PassNC_000022.10Chr2243,175,70743,382,806

    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)
    nssv186516114e-061266088
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