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nsv3067135

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:153,952

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1859 SVs from 94 studies. See in: genome view    
    Remapped(Score: Good):34,105-188,056Question Mark
    Overlapping variant regions from other studies: 1861 SVs from 94 studies. See in: genome view    
    Submitted genomic84,105-238,055Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv3067135RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1634,105188,056
    nsv3067135Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000016.9Chr1684,105238,055

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv14038734duplicationSequencingRead depth and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv14038734RemappedGoodNC_000016.10:g.341
    05_188056dup
    GRCh38.p12First PassNC_000016.10Chr1634,105188,056
    nssv14038734Submitted genomicNC_000016.9:g.8410
    5_238055dup
    GRCh37 (hg19)NC_000016.9Chr1684,105238,055

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Genotype Information

    Variant Call IDAllele Frequency (AF)
    nssv140387344.49e-005
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