Product Details

Assay Reference Genome
Location

Chr.18:52354904 on build GRCh38
Cytoband
18q21.2
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

For this assay, SNP(s) [rs72914993] 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.

Target Gene Details

Entrez Gene ID
1630
Gene Symbol
DCC
Gene Name
DCC netrin 1 receptor
Gene Aliases
CRC18, CRCR1, IGDCC1, MRMV1, NTN1R1
Location
Chr.18:52340172-53535903 on build GRCh38
Assay Gene Location
Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
DCC NM_005215.3 NP_005206.2
XM_011525843.1 XP_011524145.1
XM_017025568.1 XP_016881057.1
XM_017025569.1 XP_016881058.1
M32292.1 AAA35751.1
X76132.1 CAA53735.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
esv3583063 Chr18:52354448 - 52356219 on Build GRCh38 Loss DCC
esv275550 Chr18:52353872 - 52355816 on Build GRCh38 Loss DCC

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