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esv3810884

  • Study:estd192 (COSMIC)
  • Variant Type:copy number variation
  • Method Type:Curated
  • Submitted on:GRCh37
  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:566,763

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 1580 SVs from 79 studies. See in: genome view    
Remapped(Score: Perfect):117,077,153-117,643,915Question Mark
Overlapping variant regions from other studies: 1580 SVs from 79 studies. See in: genome view    
Submitted genomic117,834,729-118,401,491Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3810884RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2117,077,153117,077,173117,643,895117,643,915
esv3810884Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2117,834,729117,834,749118,401,471118,401,491

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16640262deletion2196280CuratedCurated221

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16640262RemappedPerfectNC_000002.12:g.(11
7077153_117077173)
_(117643895_117643
915)del
GRCh38.p12First PassNC_000002.12Chr2117,077,153117,077,173117,643,895117,643,915
essv16640262Submitted genomicNC_000002.11:g.(11
7834729_117834749)
_(118401471_118401
491)del
GRCh37 (hg19)NC_000002.11Chr2117,834,729117,834,749118,401,471118,401,491

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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