Assay Details
Target Gene Details
Entrez Gene ID: | 653319 |
Gene Name: | KIAA0895 like |
Gene Aliases: |
- |
Location: |
Chr.16:67175602-67183980 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 5 - Exon 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
KIAA0895L | NM_001040715.1 | NP_001035805.1 | ||
AK092303.1 | BAC03856.1 | |||
AK094787.1 | ||||
AK096855.1 | ||||
AL834156.1 | CAD38862.1 | |||
BC007594.1 | AAH07594.1 | |||
BC080183.1 | AAH80183.1 | |||
BC128539.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv522852 | Chr.16:67153308 - 68071571 on Build GRCh38 | Gain |
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nsv827707 | Chr.16:67148355 - 67289296 on Build GRCh38 | Loss |
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nsv952044 | Chr.16:67141198 - 67244397 on Build GRCh38 | Deletion |
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nsv1160429 | Chr.16:67161549 - 67220197 on Build GRCh38 | Deletion |
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nsv524492 | Chr.16:67174030 - 67294550 on Build GRCh38 | Loss |
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nsv524363 | Chr.16:67136529 - 68071571 on Build GRCh38 | Loss |
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More Information
Additional Information:
For this assay, SNP(s) [rs143977756] 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: |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)