diff --git a/docs/index.md b/docs/index.md
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--- a/docs/index.md
+++ b/docs/index.md
@@ -9,7 +9,7 @@ authors:
 
 <object style="float: right; width: 610px; margin-left: 15px; margin-bottom-10px; overflow: hidden" id="map" width="100%" height="500px" standby="loading data, please wait..." data="https://progenetix.org/services/geolocations?map_w_px=600&map_h_px=480&marker_type=marker&file=https://raw.githubusercontent.com/hcnv/hcnv.github.io/main/docs/contacts/people.tsv&debug=&output=map"></object>Among the different types of inherited and acquired genomic variants, regional genomic copy number variations (CNV) contribute - if measured by affected genomic sequences - contribute by far the largest amount of genomic changes, contributing both to many syndromic diseases as well as the vast majority of human cancers. The [website](http://hcnv.github.io) of the _Human Copy Number Variation Community_
 (hCNV) is a resource originated in ELIXIR's h-CNV Community Implementation Study
-(2019-2021) with the aim tpo provide a resource hub and knowledge exchange space for scientists and practitioners working with - or being interested in - genomic copy number variations in health and diseases.
+(2019-2021) with the aim to provide a resource hub and knowledge exchange space for scientists and practitioners working with - or being interested in - genomic copy number variations in health and diseases. However, the scope of the community extends beyond CNVs and includes definition of and work with other types of genomic variations with a focus on structural variants.
 
 
-## CNV News and Announcements
\ No newline at end of file
+## CNV News and Announcements