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esv3805101

  • Study:estd192 (COSMIC)
  • Variant Type:tandem duplication
  • Method Type:Curated
  • Submitted on:GRCh37
  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:421,191

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 1315 SVs from 86 studies. See in: genome view    
Remapped(Score: Perfect):99,191,198-99,612,388Question Mark
Overlapping variant regions from other studies: 1315 SVs from 86 studies. See in: genome view    
Submitted genomic99,061,929-99,483,119Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3805101RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1199,191,19899,191,21899,612,36899,612,388
esv3805101Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1199,061,92999,061,94999,483,09999,483,119

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16633841tandem duplication2186428CuratedCurated304

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16633841RemappedPerfectNC_000011.10:g.(99
191198_99191218)_(
99612368_99612388)
dup
GRCh38.p12First PassNC_000011.10Chr1199,191,19899,191,21899,612,36899,612,388
essv16633841Submitted genomicNC_000011.9:g.(990
61929_99061949)_(9
9483099_99483119)d
up
GRCh37 (hg19)NC_000011.9Chr1199,061,92999,061,94999,483,09999,483,119

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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