Hs00907703_cn

• Gene Symbol: COX6B2
• Assay Reference Genome Location: Chr.19:55350451 on build GRCh38
• Cytoband: 19q13.42

Target Gene Details

• Entrez Gene ID: 125965
• Gene Name: cytochrome c oxidase subunit 6B2
• Gene Aliases: COXVIB2, CT59
• Location: Chr.19:55349702-55354814 on Build GRCh38
• Assay Gene Location: Within Exon 5

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
COX6B2	NM_144613.4	5	914	NP_653214.2
	AK057427.1	8	1340
	BC026123.2	5	915
	BC100899.2	4	751	AAI00900.1
	BC100900.1	5	754	AAI00901.1
	BC100901.1	4	751	AAI00902.1
	BC100902.1	8	1359	AAI00903.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv953624	Chr.19:55302033 - 55625034 on Build GRCh38	Deletion	COX6B2 UBE2S TMEM150B SHISA7 KMT5C FAM71E2 ZNF865 ZNF579 FIZ1 RPL28 ZNF628 SBK2 ZNF784 BRSK1 SSC5D TMEM238 TMEM190 IL11 ZNF524 NAT14 MIR6805 SBK3 ISOC2
nsv470162	Chr.19:55334018 - 55390889 on Build GRCh38	Loss	COX6B2 TMEM150B TMEM238 KMT5C FAM71E2 TMEM190 IL11 RPL28 MIR6805
nsv516199	Chr.19:55342945 - 55389731 on Build GRCh38	Loss	COX6B2 TMEM238 KMT5C FAM71E2 TMEM190 IL11 RPL28 MIR6805

More Information

Additional Information:

For this assay, SNP(s) [rs74986603] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

• Set Membership: Intragenic, Exonic, DGV Variation

Panther Classification:

Molecular Function -

oxidase

Gene Ontology Categories:

Process(es)

hydrogen ion transmembrane transport

Function(s)

cytochrome-c oxidase activity
protein binding