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

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