Assay Details
Target Gene Details
Entrez Gene ID: | 100507053 |
Gene Name: | uncharacterized LOC100507053 |
Gene Aliases: |
- |
Location: |
Chr.4:99088857-99301356 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC100507053 | NR_037884.1 | |||
BX647987.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1002927 | Chr.4:99031321 - 99227533 on Build GRCh38 | Gain | PCNAP1 METAP1 LOC100507053 ADH6 ADH5 ADH4 |
nsv1002574 | Chr.4:99102848 - 99212536 on Build GRCh38 | Loss | PCNAP1 LOC100507053 ADH6 ADH4 |
More Information
Additional Information:
For this assay, SNP(s) [rs76124514] 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 |