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nsv7068678

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,054,963

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3145 SVs from 96 studies. See in: genome view    
    Submitted genomic20,996,324-22,051,286Question Mark
    Overlapping variant regions from other studies: 3145 SVs from 96 studies. See in: genome view    
    Remapped(Score: Perfect):21,149,258-22,204,220Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068678Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1220,996,32422,051,286
    nsv7068678RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1221,149,25822,204,220

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18751149inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18751149Submitted genomicNC_000012.12:g.209
    96324_22051286inv
    GRCh38 (hg38)NC_000012.12Chr1220,996,32422,051,286
    nssv18751149RemappedPerfectNC_000012.11:g.211
    49258_22204220inv
    GRCh37.p13First PassNC_000012.11Chr1221,149,25822,204,220

    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)
    nssv187511497e-062274536
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