Hs02157391_cn

• Gene Symbol: ZNF160
• Assay Reference Genome Location: Chr.19:53066451 on build GRCh38
• Cytoband: 19q13.41

Target Gene Details

• Entrez Gene ID: 90338
• Gene Name: zinc finger protein 160
• Gene Aliases: F11, HKr18, HZF5, KR18
• Location: Chr.19:53064882-53103434 on Build GRCh38
• Assay Gene Location: Within Exon 12

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ZNF160	XM_017027445.1	4	4731	XP_016882934.1
	XM_017027446.1	6	4692	XP_016882935.1
	AK024442.1	1	3746	BAB15732.1
	AK024789.1	1	315
	CR749613.1	1	3197	CAH18407.1
	X78928.1			CAA55528.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
esv2718787	Chr.19:52570219 - 53366454 on Build GRCh38	Deletion	VN1R2 VN1R4 ZNF320 FAM90A27P ZNF816-ZNF321P ZNF611 ZNF415 ZNF845 BIRC8 ZNF702P ZNF701 ZNF347 ZNF525 ZNF137P ERVV-2 LOC107983997 ZNF600 ZNF160 ZNF818P ZNF677 ZNF888 ZNF321P ERVV-1 LOC107985332 ZNF468 ZNF665 ZNF83 ZNF28 ZNF816
nsv428370	Chr.19:52907206 - 53149322 on Build GRCh38	Loss	LOC107985332 ERVV-2 ZNF415 ZNF816-ZNF321P ZNF160 ZNF816 ZNF888 ZNF702P ZNF321P ERVV-1 ZNF347

More Information

Additional Information:

For this assay, SNP(s) [rs112465102] 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, Exonic, DGV Variation

Panther Classification:

Molecular Function -

C2H2 zinc finger transcription factor

Gene Ontology Categories:

Process(es)

transcription, DNA-templated
regulation of transcription, DNA-templated
hemopoiesis

Function(s)

DNA binding
metal ion binding