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nsv7069551

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,587,803

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8193 SVs from 126 studies. See in: genome view    
    Submitted genomic22,654,707-24,242,509Question Mark
    Overlapping variant regions from other studies: 9096 SVs from 130 studies. See in: genome view    
    Remapped(Score: Good):22,997,177-24,638,477Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7069551Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2222,654,70724,242,509
    nsv7069551RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2222,997,17724,638,477

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18763820inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18763820Submitted genomicNC_000022.11:g.226
    54707_24242509inv
    GRCh38 (hg38)NC_000022.11Chr2222,654,70724,242,509
    nssv18763820RemappedGoodNC_000022.10:g.229
    97177_24638477inv
    GRCh37.p13First PassNC_000022.10Chr2222,997,17724,638,477

    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)
    nssv187638204e-061276268
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