Hs07544863_cn

• Gene Symbol: LOC100652833
• Assay Reference Genome Location: Chr.5:99522732 on build GRCh38
• Cytoband: 5q21.1

Target Gene Details

• Entrez Gene ID: 100652833
• Gene Name: putative POM121-like protein 1-like
• Gene Aliases: -
• Location: Chr.5:99522217-99526100 on Build GRCh38
• Assay Gene Location: Within Exon 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC100652833	XM_011543783.2	1	3369	XP_011542085.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv27807	Chr.5:99517800 - 99536729 on Build GRCh38	Gain+Loss	LOC100652833 CTD-2151A2.1
nsv1022266	Chr.5:99326944 - 99732957 on Build GRCh38	Gain	LOC100652833 CTD-2151A2.1
nsv964912	Chr.5:99521566 - 99536611 on Build GRCh38	Duplication	LOC100652833 CTD-2151A2.1
nsv599118	Chr.5:99022487 - 99693749 on Build GRCh38	Loss	LOC100652833 CTD-2151A2.1
esv3353357	Chr.5:99522049 - 99524247 on Build GRCh38	Duplication	LOC100652833
nsv1023117	Chr.5:99417695 - 99599530 on Build GRCh38	Gain	LOC100652833 CTD-2151A2.1
esv2759358	Chr.5:99269621 - 99553890 on Build GRCh38	Gain	LOC100652833 CTD-2151A2.1
nsv10726	Chr.5:99518205 - 99537200 on Build GRCh38	Loss	LOC100652833 CTD-2151A2.1
esv3575864	Chr.5:99403860 - 99574143 on Build GRCh38	Gain	LOC100652833 CTD-2151A2.1

More Information

Additional Information:

For this assay, SNP(s) [rs145676920] 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