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nsv6134122

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:287,381

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 746 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):192,927,588-193,214,968Question Mark
    Overlapping variant regions from other studies: 746 SVs from 58 studies. See in: genome view    
    Submitted genomic193,792,314-194,079,694Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv6134122RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2192,927,588192,927,590193,214,966193,214,968
    nsv6134122Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2193,792,314193,792,316194,079,692194,079,694

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17679885deletionSAMN20524657SequencingPaired-end mapping656

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv17679885RemappedPerfectNC_000002.12:g.(19
    2927588_192927590)
    _(193214966_193214
    968)del    		GRCh38.p12First PassNC_000002.12Chr2192,927,588192,927,590193,214,966193,214,968
    nssv17679885Submitted genomicNC_000002.11:g.(19
    3792314_193792316)
    _(194079692_194079
    694)del    		GRCh37 (hg19)NC_000002.11Chr2193,792,314193,792,316194,079,692194,079,694

    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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