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esv3784227

  • Study:estd192 (COSMIC)
  • Variant Type:tandem duplication
  • Method Type:Curated
  • Submitted on:GRCh37
  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:587,943

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 1498 SVs from 81 studies. See in: genome view    
Remapped(Score: Perfect):81,282,698-81,870,640Question Mark
Overlapping variant regions from other studies: 1498 SVs from 81 studies. See in: genome view    
Submitted genomic83,042,454-83,630,396Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3784227RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1081,282,69881,282,71881,870,62081,870,640
esv3784227Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr1083,042,45483,042,47483,630,37683,630,396

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16610514tandem duplication2196238CuratedCurated339

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16610514RemappedPerfectNC_000010.11:g.(81
282698_81282718)_(
81870620_81870640)
dup
GRCh38.p12First PassNC_000010.11Chr1081,282,69881,282,71881,870,62081,870,640
essv16610514Submitted genomicNC_000010.10:g.(83
042454_83042474)_(
83630376_83630396)
dup
GRCh37 (hg19)NC_000010.10Chr1083,042,45483,042,47483,630,37683,630,396

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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