Human Genome Variation
Nature Publishing Group · United Kingdom · Est. 1978
✓ Indexed in the Web of Science Core Collection (ESCI) — Clarivate publishes an official Journal Impact Factor and JCR quartile for this journal.
See the official Impact Factor & quartile on the journal’s page ↗The Impact Factor & JCR quartile are licensed by Clarivate — we link you to the official source instead of reprinting a number that can go out of date. Open metrics below: SCImago Q3. Source: Clarivate Journal Citation Reports.
Aims & Scope
Human Genome Variation is an online-only, full open access journal that contains articles and reports about variation and variability in human genomes and the consequences, implications and future impacts for the study of human genomics. An important and innovative feature of the journal is the Data Report article; these are short reports about human genome variation and variability which describe disease-causing variation and/or their frequencies. In addition, Data Reports can describe and analyse human multifactorial disease associated variations and/or their frequencies. A further feature of Human Genome Variation is a curated database of the underlying data from Data Reports, which will grow into an important resource for the genomics community. Human Genome Variation also publishes Articles and Reviews on the relevant topics in human genome studies. Full Articles is accompanied by a professionally written Editorial Summary. The intended audience for Human Genome Variation is researchers, scientists, clinicians, genetic counsellors and those interested in human genomics, from all sectors and from around the world.
General Information
Submission Info
Ethics & Quality
Think.Check.Submit Compliance
Based on the Think.Check.Submit framework by DOAJ, COPE & OASPA. All data from verified open sources.
SJR Quartile by Discipline
Scimago ranks this journal separately in each subject category — its quartile can differ by discipline.
Subject Classification
Web of Science Categories
Research Topics (OpenAlex)
Frequently asked questions about Human Genome Variation
Is Human Genome Variation a predatory journal?
PubScope has no integrity flags on record for Human Genome Variation: it is indexed in Web of Science, Scopus, DOAJ, and is not on DOAJ's withdrawn list. Its PubScope Trust Score is 74/100. Indexing is a transparency signal, not a guarantee — always confirm fit and policies before submitting.
What is the impact factor of Human Genome Variation?
Human Genome Variation is indexed in the Web of Science Core Collection, so Clarivate publishes an official Journal Impact Factor for it (since the 2023 Journal Citation Reports, every Core Collection journal — including Arts & Humanities and Emerging Sources titles — receives one). PubScope links to Clarivate's official source rather than reprinting the number, which can be out of date. Its open 2-year mean citedness is 1.41.
Is Human Genome Variation indexed in Scopus and Web of Science?
Human Genome Variation is indexed in Web of Science, Scopus, DOAJ.
What is the aims and scope of Human Genome Variation?
Human Genome Variation is an online-only, full open access journal that contains articles and reports about variation and variability in human genomes and the consequences, implications and future impacts for the study of human genomics. An important and innovative feature of the journal is the Data Report article; these are short reports about human genome variation and variability which describe disease-causing variation and/or their frequencies. In addition, Data Reports can describe and analyse human multifactorial disease associated variations and/or their frequencies. A further feature o
How much does it cost to publish in Human Genome Variation?
Human Genome Variation charges an article processing charge (APC) of about €2,790 for open-access publication.
You May Also Like
See all →Data updated: 2026-05-26 · Sources: SJR, DOAJ, OpenAlex, WoS, Crossref