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nsv6134125

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:222,806

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 552 SVs from 60 studies. See in: genome view    
    Remapped(Score: Perfect):204,770,330-204,993,135Question Mark
    Overlapping variant regions from other studies: 552 SVs from 60 studies. See in: genome view    
    Submitted genomic205,635,053-205,857,858Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv6134125RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2204,770,330204,770,332204,993,133204,993,135
    nsv6134125Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2205,635,053205,635,055205,857,856205,857,858

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17679276duplicationSAMN20524659SequencingPaired-end mapping203

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv17679276RemappedPerfectNC_000002.12:g.(20
    4770330_204770332)
    _(204993133_204993
    135)dup    		GRCh38.p12First PassNC_000002.12Chr2204,770,330204,770,332204,993,133204,993,135
    nssv17679276Submitted genomicNC_000002.11:g.(20
    5635053_205635055)
    _(205857856_205857
    858)dup    		GRCh37 (hg19)NC_000002.11Chr2205,635,053205,635,055205,857,856205,857,858

    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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