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nsv6137153

  • 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: 134 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):226,095,896-226,095,896Question Mark
    Overlapping variant regions from other studies: 86 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):73,016,536-73,016,536Question Mark
    Overlapping variant regions from other studies: 137 SVs from 22 studies. See in: genome view    
    Submitted genomic226,283,597-226,283,597Question Mark
    Overlapping variant regions from other studies: 86 SVs from 20 studies. See in: genome view    
    Submitted genomic74,776,294-74,776,294Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
    nsv6137153RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1226,095,896226,095,896+
    nsv6137153RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1073,016,53673,016,536-
    nsv6137153Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1226,283,597226,283,597+
    nsv6137153Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr1074,776,29474,776,294-

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17682570interchromosomal translocationSAMN20524662SequencingPaired-end mapping1,603

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
    nssv17682570RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1226,095,896226,095,896+
    nssv17682570RemappedPerfectGRCh38.p12First PassNC_000010.11Chr1073,016,53673,016,536-
    nssv17682570Submitted genomicGRCh37 (hg19)NC_000001.10Chr1226,283,597226,283,597+
    nssv17682570Submitted genomicGRCh37 (hg19)NC_000010.10Chr1074,776,29474,776,294-

    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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