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nsv7028985

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:135

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 77 SVs from 19 studies. See in: genome view    
    Submitted genomic26,580,021-26,580,155Question Mark
    Overlapping variant regions from other studies: 77 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):26,975,986-26,976,120Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7028985Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2226,580,02126,580,155
    nsv7028985RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2226,975,98626,976,120

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18651997duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18651997Submitted genomicNC_000022.11:g.265
    80021_26580155dup
    GRCh38 (hg38)NC_000022.11Chr2226,580,02126,580,155
    nssv18651997RemappedPerfectNC_000022.10:g.269
    75986_26976120dup
    GRCh37.p13First PassNC_000022.10Chr2226,975,98626,976,120

    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)
    nssv186519973e-057229326
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