Hs04926688_cn

• Gene Symbol: LHFPL3
• Assay Reference Genome Location: Chr.7:104349230 on build GRCh38
• Cytoband: 7q22.2

Target Gene Details

• Entrez Gene ID: 375612
• Gene Name: lipoma HMGIC fusion partner-like 3
• Gene Aliases: LHFPL4
• Location: Chr.7:104328656-104908558 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LHFPL3	NM_199000.2			NP_945351.1
	XM_005250327.1			XP_005250384.1
	AK124251.1
	AK299759.1
	AY260763.1			AAP14954.1
	BC129937.1
	BC129938.1
	BC129941.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv608065	Chr.7:104177149 - 104350307 on Build GRCh38	Gain	LHFPL3 ORC5
esv3891172	Chr.7:103796156 - 104449969 on Build GRCh38	Gain	LHFPL3 RELN ORC5
esv3614393	Chr.7:104330246 - 104360277 on Build GRCh38	Gain	LHFPL3
nsv608067	Chr.7:104303789 - 104388960 on Build GRCh38	Loss	LHFPL3

More Information

Additional Information:

For this assay, SNP(s) [rs73714805] 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, Intronic, Non-exonic, DGV Variation