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esv3809130

  • Study:estd192 (COSMIC)
  • Variant Type:complex chromosomal rearrangement
  • Method Type:Curated
  • Submitted on:GRCh37
  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 141 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):14,086,305-14,088,305Question Mark
Overlapping variant regions from other studies: 54 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):114,096,573-114,098,573Question Mark
Overlapping variant regions from other studies: 141 SVs from 36 studies. See in: genome view    
Submitted genomic14,125,930-14,127,930Question Mark
Overlapping variant regions from other studies: 54 SVs from 20 studies. See in: genome view    
Submitted genomic113,967,295-113,969,295Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3809130RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr714,086,30514,088,30514,086,30514,088,305
esv3809130RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr11114,096,573114,098,573114,096,573114,098,573
esv3809130Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr714,125,93014,127,93014,125,93014,127,930
esv3809130Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr11113,967,295113,969,295113,967,295113,969,295

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16638269interchromosomal translocation2120205CuratedCurated24

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stopstrand
essv16638269RemappedPerfectGRCh38.p12First PassNC_000007.14Chr714,086,30514,088,30514,086,30514,088,305not reported
essv16638269RemappedPerfectGRCh38.p12First PassNC_000011.10Chr11114,096,573114,098,573114,096,573114,098,573not reported
essv16638269Submitted genomicGRCh37 (hg19)NC_000007.13Chr714,125,93014,127,93014,125,93014,127,930not reported
essv16638269Submitted genomicGRCh37 (hg19)NC_000011.9Chr11113,967,295113,969,295113,967,295113,969,295not reported

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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