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University of Texas Health Science Center at Houston

Frequency of Copy Number Variants Involving The Sex Chromosomes In A Clinical Setting

Abstract

dc:description.abstract

<p>Copy number variants (CNVs) are a common finding in the clinical setting and contribute to both genetic variation as well as disease. Recently, studies have described the accumulation of multiple CNVs as a disease modifying mechanism. While it has been characterized how additional CNVs may play a role in phenotype, in which ways and to what extent sex chromosomes are involved has not been fully described. We performed a secondary data analysis using the DECIPHER database on 2,273 de-identified individuals with 2 CNVs. CNVs were designated primary and secondary based on our criteria and characteristics of both CNV groups were described. Further analysis was performed identifying differences in CNVs on the sex chromosomes vs autosomes. We found that CNVs on the sex chromosome have a significant difference compared to autosomes when comparing median size (<em>p=</em>0.013), pathogenicity classifications (<em>p<</em>0.001), and variant classification (<em>p=</em>0.001). We identified chromosome combinations for primary and secondary CNVs, and identified the X chromosome was the most common site for a secondary CNV. Additionally, we observed the plurality of secondary CNVs fell in the same chromosome as the primary CNV. From this study, we can conclude that the X chromosome is the most common site for secondary CNVs in a clinical setting. Identification of chromosome combinations for primary and secondary CNVs is essential in explanation of complex phenotypes and highlights areas of importance of the human genome.</p>

Degree

thesis:*
Name thesis:degree_name
Masters of Science (MS)
Level thesis:degree_level
Thesis (MS)
Year dc:date.available
2020

Author and committee

dc:creator, dc:contributor.*
Authors dc:creator
  • Vara, Autumn
  • <p>0000-0002-6403-8548</p>
Contributors dc:contributor
  • David Rodriguez-Buritica, M.D.
  • Syed S. Hashmi, M.D., MPH, Ph.D
  • Janice L. Smith, Ph.D

Subjects

dc:subject × 6

Identifiers

dc:identifier.*
OAI identifier oai:identifier
oai:digitalcommons.library.tmc.edu:utgsbs_dissertations-2059

Chain of custody

source
Harvested from
University of Texas Health Science Center at Houston
Base URL
digitalcommons.library.tmc.edu/do/oai/
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Vara, Autumn; <p>0000-0002-6403-8548</p>. Frequency of Copy Number Variants Involving The Sex Chromosomes In A Clinical Setting. Thesis (MS) thesis, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/1009