Assay Details
Target Gene Details
Entrez Gene ID: | 4756 |
Gene Name: | neogenin 1 |
Gene Aliases: |
IGDCC2, NGN, NTN1R2 |
Location: |
Chr.15:73051715-73305206 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv525462 | Chr.15:73057292 - 73271154 on Build GRCh38 | Loss | NEO1 |
nsv1121512 | Chr.15:72670085 - 75273877 on Build GRCh38 | Deletion | LOC105376731 FAM219B RPP25 ARID3B UBL7-AS1 COX5A C15orf59 BBS4 LOC101929333 SCAMP5 NPTN-IT1 LOC732265 MPI CPLX3 STOML1 STRA6 TBC1D21 HIGD2B MIR4513 CCDC33 CSK LOXL1-AS1 ULK3 NPTN CYP1A2 GOLGA6C ADPGK CD276 HCN4 GOLGA6A LOC102723750 C15orf39 MIR6882 ISLR PML C15orf59-AS1 ADPGK-AS1 SEMA7A CYP11A1 CYP1A1 LOC283731 REC114 NEO1 SCAMP2 LMAN1L UBL7 PPCDC LOC729739 LOC107984728 MIR6881 ISLR2 EDC3 CLK3 LOXL1 |
More Information
Additional Information:
For this assay, SNP(s) [rs78954292,rs80077473] 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 |