U.S. flag

An official website of the United States government

esv3788188

  • 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:465,838

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 1371 SVs from 91 studies. See in: genome view    
Remapped(Score: Perfect):84,166,427-84,632,264Question Mark
Overlapping variant regions from other studies: 1371 SVs from 91 studies. See in: genome view    
Submitted genomic85,078,662-85,544,499Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3788188RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr884,166,42784,166,44784,632,24484,632,264
esv3788188Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr885,078,66285,078,68285,544,47985,544,499

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16614929deletion2186066CuratedCurated446

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16614929RemappedPerfectNC_000008.11:g.(84
166427_84166447)_(
84632244_84632264)
del
GRCh38.p12First PassNC_000008.11Chr884,166,42784,166,44784,632,24484,632,264
essv16614929Submitted genomicNC_000008.10:g.(85
078662_85078682)_(
85544479_85544499)
del
GRCh37 (hg19)NC_000008.10Chr885,078,66285,078,68285,544,47985,544,499

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

Support Center