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esv3769730

  • 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:477,281

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 2062 SVs from 102 studies. See in: genome view    
Remapped(Score: Perfect):10,065,611-10,542,891Question Mark
Overlapping variant regions from other studies: 2064 SVs from 102 studies. See in: genome view    
Submitted genomic10,065,611-10,542,891Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3769730RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr910,065,61110,065,63110,542,87110,542,891
esv3769730Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr910,065,61110,065,63110,542,87110,542,891

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16594397deletion2197375CuratedCurated21

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16594397RemappedPerfectNC_000009.12:g.(10
065611_10065631)_(
10542871_10542891)
del
GRCh38.p12First PassNC_000009.12Chr910,065,61110,065,63110,542,87110,542,891
essv16594397Submitted genomicNC_000009.11:g.(10
065611_10065631)_(
10542871_10542891)
del
GRCh37 (hg19)NC_000009.11Chr910,065,61110,065,63110,542,87110,542,891

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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