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nsv7062736

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,630,210

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 21076 SVs from 119 studies. See in: genome view    
    Submitted genomic36,955,253-45,585,462Question Mark
    Overlapping variant regions from other studies: 21084 SVs from 119 studies. See in: genome view    
    Remapped(Score: Good):35,583,656-44,214,101Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7062736Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2036,955,25345,585,462
    nsv7062736RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2035,583,65644,214,101

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18762340inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18762340Submitted genomicNC_000020.11:g.369
    55253_45585462inv
    GRCh38 (hg38)NC_000020.11Chr2036,955,25345,585,462
    nssv18762340RemappedGoodNC_000020.10:g.355
    83656_44214101inv
    GRCh37.p13First PassNC_000020.10Chr2035,583,65644,214,101

    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)
    nssv187623400.001300274544
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