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nsv6137546

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

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 167 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):1,404,569-1,404,569Question Mark
    Overlapping variant regions from other studies: 78 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):68,276,157-68,276,157Question Mark
    Overlapping variant regions from other studies: 167 SVs from 19 studies. See in: genome view    
    Submitted genomic1,404,804-1,404,804Question Mark
    Overlapping variant regions from other studies: 78 SVs from 20 studies. See in: genome view    
    Submitted genomic68,043,625-68,043,625Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
    nsv6137546RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr61,404,5691,404,569+
    nsv6137546RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1168,276,15768,276,157+
    nsv6137546Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr61,404,8041,404,804+
    nsv6137546Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1168,043,62568,043,625+

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17682632interchromosomal translocationSAMN20524665SequencingPaired-end mapping405

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
    nssv17682632RemappedPerfectGRCh38.p12First PassNC_000006.12Chr61,404,5691,404,569+
    nssv17682632RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1168,276,15768,276,157+
    nssv17682632Submitted genomicGRCh37 (hg19)NC_000006.11Chr61,404,8041,404,804+
    nssv17682632Submitted genomicGRCh37 (hg19)NC_000011.9Chr1168,043,62568,043,625+

    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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