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nsv7073053

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,318

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 116 SVs from 20 studies. See in: genome view    
    Submitted genomic87,951,800-87,954,117Question Mark
    Overlapping variant regions from other studies: 116 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):88,495,031-88,497,348Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073053Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1587,951,80087,954,117
    nsv7073053RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1588,495,03188,497,348

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756079inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756079Submitted genomicNC_000015.10:g.879
    51800_87954117inv
    GRCh38 (hg38)NC_000015.10Chr1587,951,80087,954,117
    nssv18756079RemappedPerfectNC_000015.9:g.8849
    5031_88497348inv
    GRCh37.p13First PassNC_000015.9Chr1588,495,03188,497,348

    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)
    nssv187560791.4e-054275898
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