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nsv7099231

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,043,693

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3210 SVs from 86 studies. See in: genome view    
    Remapped(Score: Good):149,962,894-151,006,586Question Mark
    Overlapping variant regions from other studies: 3296 SVs from 90 studies. See in: genome view    
    Submitted genomic149,934,818-150,979,062Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
    nsv7099231RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1149,962,894151,006,586
    nsv7099231Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1149,934,818150,979,062

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18792964duplicationSNP arraySNP genotyping analysis

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
    nssv18792964RemappedGoodNC_000001.11:g.(14
    9962894_?)_(?_1510
    06586)dup
    GRCh38.p12First PassNC_000001.11Chr1149,962,894151,006,586
    nssv18792964Submitted genomicNC_000001.10:g.(14
    9934818_?)_(?_1509
    79062)dup
    GRCh37 (hg19)NC_000001.10Chr1149,934,818150,979,062

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    No genotype data were submitted for this variant

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