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nsv7070485

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,032,352

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3084 SVs from 96 studies. See in: genome view    
    Submitted genomic21,009,516-22,041,867Question Mark
    Overlapping variant regions from other studies: 3084 SVs from 96 studies. See in: genome view    
    Remapped(Score: Perfect):21,162,450-22,194,801Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070485Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1221,009,51622,041,867
    nsv7070485RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1221,162,45022,194,801

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18751150inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18751150Submitted genomicNC_000012.12:g.210
    09516_22041867inv
    GRCh38 (hg38)NC_000012.12Chr1221,009,51622,041,867
    nssv18751150RemappedPerfectNC_000012.11:g.211
    62450_22194801inv
    GRCh37.p13First PassNC_000012.11Chr1221,162,45022,194,801

    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)
    nssv18751150<0.00132272024
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