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nsv7047209

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,189,385

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 13150 SVs from 116 studies. See in: genome view    
    Submitted genomic222,803,564-227,992,948Question Mark
    Overlapping variant regions from other studies: 13150 SVs from 116 studies. See in: genome view    
    Remapped(Score: Perfect):223,668,283-228,857,664Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047209Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2222,803,564227,992,948
    nsv7047209RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2223,668,283228,857,664

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18768047inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18768047Submitted genomicNC_000002.12:g.222
    803564_227992948in
    v
    GRCh38 (hg38)NC_000002.12Chr2222,803,564227,992,948
    nssv18768047RemappedPerfectNC_000002.11:g.223
    668283_228857664in
    v
    GRCh37.p13First PassNC_000002.11Chr2223,668,283228,857,664

    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)
    nssv187680474e-061276268
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