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esv3805924

  • Study:estd192 (COSMIC)
  • Variant Type:tandem duplication
  • Method Type:Curated
  • Submitted on:GRCh37
  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50,462,537

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 119288 SVs from 143 studies. See in: genome view    
Remapped(Score: Good):8,103,212-58,565,748Question Mark
Overlapping variant regions from other studies: 119140 SVs from 143 studies. See in: genome view    
Submitted genomic8,144,899-58,551,475Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3805924RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr38,103,2128,103,21258,565,74858,565,748
esv3805924Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr38,144,8998,144,91958,551,45558,551,475

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16634706tandem duplication2196256CuratedCurated308

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16634706RemappedGoodNC_000003.12:g.(81
03212_8103212)_(58
565748_58565748)du
p
GRCh38.p12First PassNC_000003.12Chr38,103,2128,103,21258,565,74858,565,748
essv16634706Submitted genomicNC_000003.11:g.(81
44899_8144919)_(58
551455_58551475)du
p
GRCh37 (hg19)NC_000003.11Chr38,144,8998,144,91958,551,45558,551,475

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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