Hs04015517_cn

• Gene Symbol: ZNF350-AS1
• Assay Reference Genome Location: Chr.19:51958937 on build GRCh38
• Cytoband: 19q13.41

Target Gene Details

• Entrez Gene ID: 101669766
• Gene Name: ZNF350 antisense RNA 1
• Gene Aliases: HCCAT3, uc002pyc
• Location: Chr.19:51949134-51981367 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ZNF350-AS1	NR_103847.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv580006	Chr.19:51946390 - 52016355 on Build GRCh38	Loss	ZNF350-AS1 ZNF615 ZNF350 ZNF614
nsv833872	Chr.19:51928534 - 52115771 on Build GRCh38	Loss	ZNF613 ZNF432 ZNF350-AS1 ZNF841 ZNF615 ZNF350 ZNF616 ZNF614
dgv425n27	Chr.19:51784199 - 52104512 on Build GRCh38	Gain	ZNF613 ZNF432 ZNF350-AS1 ZNF841 LOC100419706 ZNF615 ZNF649 ZNF350 ZNF649-AS1 ZNF614 ZNF577 FPR3
dgv1067e212	Chr.19:51768056 - 52117340 on Build GRCh38	Gain	ZNF432 ZNF350-AS1 ZNF649 ZNF350 ZNF616 ZNF649-AS1 FPR3 ZNF613 ZNF841 LOC100419706 ZNF615 FPR2 ZNF614 ZNF577
dgv143e55	Chr.19:51724663 - 52127682 on Build GRCh38	Gain	ZNF432 ZNF350-AS1 ZNF649 ZNF350 ZNF616 ZNF649-AS1 FPR3 ZNF613 ZNF841 LOC100419706 ZNF615 FPR1 FPR2 ZNF614 ZNF577
esv2758767	Chr.19:51488642 - 52101372 on Build GRCh38	Gain+Loss	ZNF350-AS1 ZNF649 FPR3 LOC100419706 CEACAM18 ZNF615 SIGLEC14 SPACA6 FPR1 SIGLEC6 SIGLEC12 MIRLET7E SIGLEC5 ZNF175 ZNF432 SPACA6P-AS MIR99B ZNF350 ZNF649-AS1 HAS1 ZNF613 ZNF841 MIR125A LOC339352 FPR2 ZNF614 ZNF577 LINC01530
nsv580001	Chr.19:51798407 - 52013985 on Build GRCh38	Gain	ZNF613 ZNF350-AS1 LOC100419706 ZNF615 ZNF649 ZNF350 ZNF649-AS1 ZNF614 ZNF577 FPR3
dgv3626n100	Chr.19:51746647 - 52125358 on Build GRCh38	Gain	ZNF432 ZNF350-AS1 ZNF649 ZNF350 ZNF616 ZNF649-AS1 FPR3 ZNF613 ZNF841 LOC100419706 ZNF615 FPR1 FPR2 ZNF614 ZNF577
dgv6523n54	Chr.19:51767689 - 52118391 on Build GRCh38	Gain	ZNF432 ZNF350-AS1 ZNF649 ZNF350 ZNF616 ZNF649-AS1 FPR3 ZNF613 ZNF841 LOC100419706 ZNF615 FPR2 ZNF614 ZNF577

More Information

Additional Information:

For this assay, SNP(s) [rs141061313] 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