Hs03968641_cn

• Gene Symbol: LOC100130950
• Assay Reference Genome Location: Chr.17:5201256 on build GRCh38
• Cytoband: 17p13.2

Target Gene Details

• Entrez Gene ID: 100130950
• Gene Name: uncharacterized LOC100130950
• Gene Aliases: -
• Location: Chr.17:5192084-5235636 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC100130950	NR_034082.1
	AK021878.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv574273	Chr.17:4585589 - 5460332 on Build GRCh38	Gain	SLC52A1 LOC101559451 LOC100130950 ZNF594 LOC102724009 ARRB2 ZMYND15 MIR6864 INCA1 VMO1 GLTPD2 MED11 CAMTA2 DHX33 RPAIN MIR6865 ALOX15 USP6 SCIMP ZNF232 GP1BA C17orf107 ENO3 RNF167 LOC101927979 SLC25A11 KIF1C CHRNE NUP88 PSMB6 ZFP3 PFN1 LOC400568 SMTNL2 RABEP1 CXCL16 PLD2 LOC107984973 SPAG7 LOC101928000 PELP1 MINK1 C1QBP TM4SF5
dgv3089n100	Chr.17:5187013 - 5327634 on Build GRCh38	Gain	RABEP1 LOC100130950 ZNF594 SCIMP

More Information

Additional Information:

For this assay, SNP(s) [rs73333445] 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