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nsv7027228

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 158 SVs from 36 studies. See in: genome view    
    Submitted genomic43,153,014-43,153,085Question Mark
    Overlapping variant regions from other studies: 158 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):43,549,020-43,549,091Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7027228Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2243,153,01443,153,085
    nsv7027228RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2243,549,02043,549,091

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18652253duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18652253Submitted genomicNC_000022.11:g.431
    53014_43153085dup
    GRCh38 (hg38)NC_000022.11Chr2243,153,01443,153,085
    nssv18652253RemappedPerfectNC_000022.10:g.435
    49020_43549091dup
    GRCh37.p13First PassNC_000022.10Chr2243,549,02043,549,091

    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)
    nssv186522530.2744986169064
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