<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sharma NK</submitter><funding>Indian Council of Agricultural Research, Ministry of Agriculture and Farmers’ Welfare, Govt. of India</funding><pagination>2446251</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12674279</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>36(1)</volume><pubmed_abstract>Copy number variations (CNVs) have become widely acknowledged as a significant source of genomic variability and phenotypic variance. To understand the genetic variants in horses, CNVs from six Indian horse breeds, &lt;i>namely,&lt;/i> Manipuri, Zanskari, Bhutia, Spiti, Kathiawari and Marwari were discovered using Axiom&lt;sup>™&lt;/sup> Equine Genotyping Array. These breeds differed in agro-climatic adaptation with distinct phenotypic characters. A total of 2668 autosomal CNVs and 381 CNV regions (CNVRs) were identified with PennCNV tool. DeepCNV was employed to re-validate to get 883 autosomal CNVs, of which 9.06% were singleton type. A total of 180 CNVRs were identified after DeepCNV filtering with the estimated length of 3.12 Kb-4.90 Mb. The functional analysis showed the majority of the CNVRs genes enriched for sensory perception and olfactory receptor activity. An Equine CNVs database, EqCNVdb (http://backlin.cabgrid.res.in/eqcnvdb/) was developed which catalogues detailed information on the horse CNVs, CNVRs and gene content within CNVRs. Also, three random CNVRs were validated with real-time polymerase chain reaction. These findings will aid in the understanding the horse genome and serve as a preliminary foundation for future CNV association research with commercially significant equine traits. The identification of CNVs and CNVRs would lead to better insights into genetic basis of important traits.</pubmed_abstract><journal>Animal biotechnology</journal><pubmed_title>Genome wide landscaping of copy number variations for horse inter-breed variability.</pubmed_title><pmcid>PMC12674279</pmcid><funding_grant_id>-A&amp;amp;P</funding_grant_id><funding_grant_id>Agril. Edn.4-1/</funding_grant_id><pubmed_authors>Saha B</pubmed_authors><pubmed_authors>Pal Y</pubmed_authors><pubmed_authors>Giri SK</pubmed_authors><pubmed_authors>Bhattacharya TK</pubmed_authors><pubmed_authors>Bhardwaj A</pubmed_authors><pubmed_authors>Rai A</pubmed_authors><pubmed_authors>Nayan V</pubmed_authors><pubmed_authors>Legha RA</pubmed_authors><pubmed_authors>Kumar D</pubmed_authors><pubmed_authors>Jaiswal S</pubmed_authors><pubmed_authors>Iquebal MA</pubmed_authors><pubmed_authors>Sharma NK</pubmed_authors><pubmed_authors>Singh P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genome wide landscaping of copy number variations for horse inter-breed variability.</name><description>Copy number variations (CNVs) have become widely acknowledged as a significant source of genomic variability and phenotypic variance. To understand the genetic variants in horses, CNVs from six Indian horse breeds, &lt;i>namely,&lt;/i> Manipuri, Zanskari, Bhutia, Spiti, Kathiawari and Marwari were discovered using Axiom&lt;sup>™&lt;/sup> Equine Genotyping Array. These breeds differed in agro-climatic adaptation with distinct phenotypic characters. A total of 2668 autosomal CNVs and 381 CNV regions (CNVRs) were identified with PennCNV tool. DeepCNV was employed to re-validate to get 883 autosomal CNVs, of which 9.06% were singleton type. A total of 180 CNVRs were identified after DeepCNV filtering with the estimated length of 3.12 Kb-4.90 Mb. The functional analysis showed the majority of the CNVRs genes enriched for sensory perception and olfactory receptor activity. An Equine CNVs database, EqCNVdb (http://backlin.cabgrid.res.in/eqcnvdb/) was developed which catalogues detailed information on the horse CNVs, CNVRs and gene content within CNVRs. Also, three random CNVRs were validated with real-time polymerase chain reaction. These findings will aid in the understanding the horse genome and serve as a preliminary foundation for future CNV association research with commercially significant equine traits. The identification of CNVs and CNVRs would lead to better insights into genetic basis of important traits.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-30T03:25:15.71Z</modification><creation>2026-06-30T03:20:27.846Z</creation></dates><accession>S-EPMC12674279</accession><cross_references><pubmed>39791493</pubmed><doi>10.1080/10495398.2024.2446251</doi></cross_references></HashMap>