diff --git a/CHANGELOG.md b/CHANGELOG.md
index 8c794ad696..7d5c8c88ff 100644
--- a/CHANGELOG.md
+++ b/CHANGELOG.md
@@ -46,6 +46,7 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0
 - [#1177](https://github.com/nf-core/sarek/pull/1177) - Fix status inference when using nf-validation plugin
 - [#1183](https://github.com/nf-core/sarek/pull/1183) - Add docs for concatentated germline variants
 - [#1184](https://github.com/nf-core/sarek/pull/1184) - Fix issue with duplicated variants in VCF from Sentieon-based joint-germline variant-calling with VQSR. (Corresponding to [#966](https://github.com/nf-core/sarek/issues/966) for GATK.)
+- [#1192](https://github.com/nf-core/sarek/pull/1192) - Add `ASCATprofile.png` to ASCAT output docs
 
 ### Dependencies
 
diff --git a/docs/output.md b/docs/output.md
index a39a728018..9f90bac28c 100644
--- a/docs/output.md
+++ b/docs/output.md
@@ -598,6 +598,8 @@ This is done internally using the software [AlleleCount](https://github.com/canc
 
 **Output directory: `{outdir}/variantcalling/ascat/<tumorsample_vs_normalsample>/`**
 
+- `<tumorsample_vs_normalsample>.tumour.ASCATprofile.png`
+  - image with information about allele-specific copy number profile
 - `<tumorsample_vs_normalsample>.tumour.ASPCF.png`
   - image with information about allele-specific copy number segmentation
 - `<tumorsample_vs_normalsample>.before_correction_Tumour.<tumorsample_vs_normalsample>.tumour.png`