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nsv7140287

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:95

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 130 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):34,102,573-34,102,667Question Mark
    Overlapping variant regions from other studies: 130 SVs from 43 studies. See in: genome view    
    Submitted genomic34,568,174-34,568,268Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7140287RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr134,102,57334,102,667
    nsv7140287Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr134,568,17434,568,268

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18835152deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18835152RemappedPerfectNC_000001.11:g.341
    02573_34102667del
    GRCh38.p12First PassNC_000001.11Chr134,102,57334,102,667
    nssv18835152Submitted genomicNC_000001.10:g.345
    68174_34568268del
    GRCh37.p13NC_000001.10Chr134,568,17434,568,268

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv188351520.524
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