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nsv6134773

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:46,180

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 210 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):175,493,237-175,539,416Question Mark
    Overlapping variant regions from other studies: 45 SVs from 18 studies. See in: genome view    
    Remapped(Score: Pass):166,749-197,752Question Mark
    Overlapping variant regions from other studies: 210 SVs from 44 studies. See in: genome view    
    Submitted genomic175,211,025-175,257,204Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv6134773RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3175,493,237175,493,238175,539,403175,539,416
    nsv6134773RemappedPassGRCh38.p12PATCHESSecond PassNW_019805489.1Chr3|NW_01
    9805489.1
    166,749166,750197,752-
    nsv6134773Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3175,211,025175,211,026175,257,191175,257,204

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17680238inversionSAMN20524658SequencingPaired-end mapping48

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv17680238RemappedPassNW_019805489.1:g.(
    166749_166750)_(19
    7752_?)inv
    GRCh38.p12Second PassNW_019805489.1Chr3|NW_01
    9805489.1
    166,749166,750197,752-
    nssv17680238RemappedPerfectNC_000003.12:g.(17
    5493237_175493238)
    _(175539403_175539
    416)inv
    GRCh38.p12First PassNC_000003.12Chr3175,493,237175,493,238175,539,403175,539,416
    nssv17680238Submitted genomicNC_000003.11:g.(17
    5211025_175211026)
    _(175257191_175257
    204)inv
    GRCh37 (hg19)NC_000003.11Chr3175,211,025175,211,026175,257,191175,257,204

    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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