nsv6137175

  • 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: 126 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):27,664,692-27,664,692Question Mark
    Overlapping variant regions from other studies: 77 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):68,275,622-68,275,622Question Mark
    Overlapping variant regions from other studies: 126 SVs from 37 studies. See in: genome view    
    Submitted genomic27,632,471-27,632,471Question Mark
    Overlapping variant regions from other studies: 77 SVs from 20 studies. See in: genome view    
    Submitted genomic68,043,090-68,043,090Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
    nsv6137175RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr627,664,69227,664,692+
    nsv6137175RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1168,275,62268,275,622-
    nsv6137175Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr627,632,47127,632,471+
    nsv6137175Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1168,043,09068,043,090-

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17677392interchromosomal translocationSAMN20524665SequencingPaired-end mapping405

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
    nssv17677392RemappedPerfectGRCh38.p12First PassNC_000006.12Chr627,664,69227,664,692+
    nssv17677392RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1168,275,62268,275,622-
    nssv17677392Submitted genomicGRCh37 (hg19)NC_000006.11Chr627,632,47127,632,471+
    nssv17677392Submitted genomicGRCh37 (hg19)NC_000011.9Chr1168,043,09068,043,090-

    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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