Hs01692266_cn

• Gene Symbol: KIAA0895L
• Assay Reference Genome Location: Chr.16:67178091 on build GRCh38
• Cytoband: 16q22.1

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	C16orf86 CTCF LOC100505942 LOC107984813 FAM65A DUS2 TMEM208 FBXL8 ENKD1 DDX28 HSF4 FHOD1 GFOD2 LRRC36 RANBP10 CARMIL2 ELMO3 TPPP3 NUTF2 SLC9A5 THAP11 PARD6A NOL3 LRRC29 ACD TRADD PSMB10 ZDHHC1 DPEP3 TSNAXIP1 MIR328 LOC105369155 PSKH1 EXOC3L1 KCTD19 NRN1L ATP6V0D1 AGRP LOC100131303 SLC12A4 KIAA0895L HSD11B2 LCAT CENPT PLEKHG4 E2F4 DPEP2 EDC4 CTRL
nsv827707	Chr.16:67148355 - 67289296 on Build GRCh38	Loss	FBXL8 LRRC29 B3GNT9 C16orf70 TRADD HSF4 FHOD1 KIAA0895L MIR328 ELMO3 LOC105369155 PLEKHG4 E2F4 SLC9A5 EXOC3L1 TMEM208 NOL3
nsv952044	Chr.16:67141198 - 67244397 on Build GRCh38	Deletion	FBXL8 LRRC29 B3GNT9 C16orf70 TRADD HSF4 FHOD1 KIAA0895L MIR328 ELMO3 LOC105369155 E2F4 EXOC3L1 TMEM208 NOL3
nsv1160429	Chr.16:67161549 - 67220197 on Build GRCh38	Deletion	MIR328 ELMO3 FBXL8 LOC105369155 LRRC29 E2F4 HSF4 KIAA0895L EXOC3L1 NOL3
nsv524492	Chr.16:67174030 - 67294550 on Build GRCh38	Loss	LRRC29 FHOD1 KIAA0895L MIR328 ELMO3 LOC105369155 PLEKHG4 E2F4 SLC9A5 EXOC3L1 KCTD19 TMEM208 NOL3
nsv524363	Chr.16:67136529 - 68071571 on Build GRCh38	Loss	C16orf86 CTCF LOC100505942 LOC107984813 FAM65A DUS2 TMEM208 FBXL8 B3GNT9 ENKD1 DDX28 HSF4 FHOD1 GFOD2 LRRC36 RANBP10 CARMIL2 ELMO3 TPPP3 NUTF2 SLC9A5 THAP11 PARD6A NOL3 LRRC29 ACD TRADD PSMB10 ZDHHC1 DPEP3 TSNAXIP1 MIR328 LOC105369155 PSKH1 EXOC3L1 KCTD19 NRN1L ATP6V0D1 C16orf70 AGRP LOC100131303 SLC12A4 KIAA0895L HSD11B2 LCAT CENPT PLEKHG4 E2F4 DPEP2 EDC4 CTRL

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: Intragenic, Non-exonic, DGV Variation