Product Details

Assay Reference Genome
Location

Chr.20:15931863 on build GRCh38
Cytoband
20p12.1
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

For this assay, SNP(s) [rs75206496] 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
613266
Gene Symbol
LOC613266
Gene Name
uncharacterized LOC613266
Gene Aliases
Location
Chr.20:15892333-15985882 on build GRCh38
Assay Gene Location
Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
LOC613266 NR_130924.1
DA380977.1
Entrez Gene ID
140733
Gene Symbol
MACROD2
Gene Name
MACRO domain containing 2
Gene Aliases
C20orf133
Location
Chr.20:13995476-16053197 on build GRCh38
Assay Gene Location
Within Intron 12
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
MACROD2 NM_001033087.1 NP_001028259.1
NM_080676.5 NP_542407.2
XM_017027675.1 XP_016883164.1
XM_017027676.1 XP_016883165.1
XM_017027677.1 XP_016883166.1
AK125899.1
AK131348.1 BAD18504.1
BC018687.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
nsv1057333 Chr20:15088323 - 16315570 on Build GRCh38 Gain LOC613266 KIF16B MACROD2
nsv833929 Chr20:15784727 - 15996692 on Build GRCh38 Gain LOC613266 MACROD2
nsv3304 Chr20:15927189 - 15962052 on Build GRCh38 Insertion LOC613266 MACROD2

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