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nsv3067124

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,280

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 402 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):177,122-178,401Question Mark
    Overlapping variant regions from other studies: 402 SVs from 52 studies. See in: genome view    
    Submitted genomic227,121-228,400Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv3067124RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr16177,122178,401
    nsv3067124Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000016.9Chr16227,121228,400

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv14038746deletionSequencingRead depth and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv14038746RemappedPerfectNC_000016.10:g.177
    122_178401del
    GRCh38.p12First PassNC_000016.10Chr16177,122178,401
    nssv14038746Submitted genomicNC_000016.9:g.2271
    21_228400del
    GRCh37 (hg19)NC_000016.9Chr16227,121228,400

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Genotype Information

    Variant Call IDAllele Frequency (AF)
    nssv140387464.49e-005
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