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nsv7069393

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,606,622

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9803 SVs from 125 studies. See in: genome view    
    Submitted genomic53,026,789-54,633,410Question Mark
    Overlapping variant regions from other studies: 5763 SVs from 113 studies. See in: genome view    
    Remapped(Score: Pass):53,530,042-54,528,887Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7069393Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1953,026,78954,633,410
    nsv7069393RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1953,530,04254,528,887

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760677inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760677Submitted genomicNC_000019.10:g.530
    26789_54633410inv
    GRCh38 (hg38)NC_000019.10Chr1953,026,78954,633,410
    nssv18760677RemappedPassNC_000019.9:g.5353
    0042_54528887inv
    GRCh37.p13First PassNC_000019.9Chr1953,530,04254,528,887

    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)
    nssv187606774e-061276268
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