nsv6136292

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,029

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 202 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):38,298,299-38,330,327Question Mark
    Overlapping variant regions from other studies: 202 SVs from 29 studies. See in: genome view    
    Submitted genomic38,155,817-38,187,845Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nsv6136292RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr838,298,29938,298,31238,330,31838,330,327
    nsv6136292Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr838,155,81738,155,83038,187,83638,187,845

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv17680306inversionSAMN20524664SequencingPaired-end mapping739

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
    nssv17680306RemappedPerfectNC_000008.11:g.(38
    298299_38298312)_(
    38330318_38330327)
    inv    		GRCh38.p12First PassNC_000008.11Chr838,298,29938,298,31238,330,31838,330,327
    nssv17680306Submitted genomicNC_000008.10:g.(38
    155817_38155830)_(
    38187836_38187845)
    inv    		GRCh37 (hg19)NC_000008.10Chr838,155,81738,155,83038,187,83638,187,845

    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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