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esv4011080

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,001

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 365 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):11,736,294-11,737,294Question Mark
    Overlapping variant regions from other studies: 366 SVs from 24 studies. See in: genome view    
    Submitted genomic13,857,000-13,858,000Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    esv4011080RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000024.10ChrY11,736,29411,737,294
    esv4011080Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000024.9ChrY13,857,00013,858,000

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
    essv26067087copy number gainhepG2SequencingRead depth and paired-end mapping51,026

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    essv26067087RemappedPerfectNC_000024.10:g.117
    36294_11737294dup
    GRCh38.p12First PassNC_000024.10ChrY11,736,29411,737,294
    essv26067087Submitted genomicNC_000024.9:g.1385
    7000_13858000dup10
    00
    GRCh37 (hg19)NC_000024.9ChrY13,857,00013,858,000

    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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