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esv3781932

  • 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:570,378

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 1581 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):65,112,504-65,682,881Question Mark
Overlapping variant regions from other studies: 1581 SVs from 78 studies. See in: genome view    
Submitted genomic65,686,636-66,257,013Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3781932RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1365,112,50465,112,52465,682,86165,682,881
esv3781932Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1365,686,63665,686,65666,256,99366,257,013

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16607992deletion2121185CuratedCurated55

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16607992RemappedPerfectNC_000013.11:g.(65
112504_65112524)_(
65682861_65682881)
del
GRCh38.p12First PassNC_000013.11Chr1365,112,50465,112,52465,682,86165,682,881
essv16607992Submitted genomicNC_000013.10:g.(65
686636_65686656)_(
66256993_66257013)
del
GRCh37 (hg19)NC_000013.10Chr1365,686,63665,686,65666,256,99366,257,013

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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