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See other LOC105369205 CNV Assays ›
Gene Symbol
LOC105369205
Assay Reference Genome
Location

Chr.17:20951258 on build GRCh38
Cytoband
17p11.2
Assay ID Hs06421103_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 105369205

Gene Name:

 uncharacterized LOC105369205

Gene Aliases:

 -

Location:

 Chr.17:20921016-21001059 on Build GRCh38

Assay Gene Location:
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LOC105369205

Target Gene Details

Entrez Gene ID:

 339260

Gene Name:

 uncharacterized LOC339260

Gene Aliases:

 -

Location:

 Chr.17:20938520-20982357 on Build GRCh38

Assay Gene Location:

 Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LOC339260 NR_123730.1
DB066214.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1064365 Chr.17:20898426 - 20987403 on Build GRCh38 Gain CCDC144NL-AS1 LOC339260 LOC105369205
dgv5502n54 Chr.17:20899465 - 20969018 on Build GRCh38 Gain CCDC144NL-AS1 LOC339260 LOC105369205
esv2751619 Chr.17:20559595 - 21010843 on Build GRCh38 Gain USP22 CDRT15L2 CCDC144NL-AS1 LOC339260 LOC105369205 MEIS3P2 ABHD17AP6 CCDC144NL LOC100287072
nsv1059146 Chr.17:20849194 - 22546654 on Build GRCh38 Gain LINC01563 DHRS7B LOC100996792 FLJ36000 LOC339260 NATD1 UBBP4 KCNJ12 CCDC144NL MAP2K3 USP22 TMEM11 CCDC144NL-AS1 MTRNR2L1 FAM27E5 LOC105369205 C17orf51 KCNJ18
esv3640221 Chr.17:20913840 - 20955637 on Build GRCh38 Loss LOC339260 LOC105369205
nsv457706 Chr.17:20911453 - 20969018 on Build GRCh38 Gain LOC339260 LOC105369205
nsv2006 Chr.17:20943450 - 20989417 on Build GRCh38 Deletion LOC339260 LOC105369205

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More Information


Additional Information:

For this assay, SNP(s) [rs78880025] 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

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