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esv3814945

  • Study:estd192 (COSMIC)
  • Variant Type:tandem duplication
  • Method Type:Curated
  • Submitted on:GRCh37
  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,610,195

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 65893 SVs from 144 studies. See in: genome view    
Remapped(Score: Good):34,867,223-63,477,417Question Mark
Overlapping variant regions from other studies: 65862 SVs from 144 studies. See in: genome view    
Submitted genomic34,908,715-63,463,093Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3814945RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr334,867,22334,867,22363,477,41763,477,417
esv3814945Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr334,908,71534,908,73563,463,07363,463,093

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16644797tandem duplication2186428CuratedCurated304

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16644797RemappedGoodNC_000003.12:g.(34
867223_34867223)_(
63477417_63477417)
dup
GRCh38.p12First PassNC_000003.12Chr334,867,22334,867,22363,477,41763,477,417
essv16644797Submitted genomicNC_000003.11:g.(34
908715_34908735)_(
63463073_63463093)
dup
GRCh37 (hg19)NC_000003.11Chr334,908,71534,908,73563,463,07363,463,093

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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