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nsv7067872

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:400,741

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1177 SVs from 72 studies. See in: genome view    
    Submitted genomic28,416,471-28,817,211Question Mark
    Overlapping variant regions from other studies: 862 SVs from 62 studies. See in: genome view    
    Remapped(Score: Pass):26,840,020-27,144,229Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067872Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1728,416,47128,817,211
    nsv7067872RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1726,840,02027,144,229

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756922inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756922Submitted genomicNC_000017.11:g.284
    16471_28817211inv
    GRCh38 (hg38)NC_000017.11Chr1728,416,47128,817,211
    nssv18756922RemappedPassNC_000017.10:g.268
    40020_27144229inv
    GRCh37.p13First PassNC_000017.10Chr1726,840,02027,144,229

    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)
    nssv187569223.2e-055275612
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