Article

PanCNV-Explorer: Deciphering copy number alterations across human cancers

2026-01-27

Abstract excerpt

Copy number variants (CNVs) are major drivers of cancer progression and genetic disorders, yet their interpretation, spanning biological mechanisms, clinical relevance, and therapeutic implications, remains fragmented across disparate resources. To bridge this gap, we present PanCNV-Explorer, a unified database integrating harmonized copy number variation data across 33 cancer types, cancer cell lines, and healthy...

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Literature Corpus work: 8a8d334d-726b-5dd1-ae4d-0a3408b8d898
DOI: 10.64898/2026.01.26.701884

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