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See other ANKRD20A19P CNV Assays ›
Gene Symbol
ANKRD20A19P
Assay Reference Genome
Location

Chr.13:23924284 on build GRCh38
Cytoband
13q12.12
Assay ID Hs03850235_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 400110

Gene Name:

 ankyrin repeat domain 20 family member A19, pseudogene

Gene Aliases:

 -

Location:

 Chr.13:23907284-23949315 on Build GRCh38

Assay Gene Location:

 Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
ANKRD20A19P NR_073430.1
AK127292.1 BAC86920.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv525965 Chr.13:22937442 - 24358507 on Build GRCh38 Gain C1QTNF9B-AS1 ANKRD20A19P C1QTNF9B MIPEP SPATA13-AS1 MIR2276 LINC00327 SGCG SACS SACS-AS1 NUS1P3 LINC00566 TNFRSF19 C1QTNF9 SPATA13
nsv561338 Chr.13:23901934 - 24051027 on Build GRCh38 Gain ANKRD20A19P SPATA13
nsv561292 Chr.13:23025847 - 24348376 on Build GRCh38 Loss C1QTNF9B-AS1 ANKRD20A19P C1QTNF9B MIPEP SPATA13-AS1 MIR2276 LINC00327 SGCG SACS SACS-AS1 NUS1P3 LINC00566 TNFRSF19 C1QTNF9 SPATA13
dgv3084n54 Chr.13:22925582 - 24378278 on Build GRCh38 Gain C1QTNF9B-AS1 ANKRD20A19P C1QTNF9B MIPEP SPATA13-AS1 MIR2276 LINC00327 SGCG SACS SACS-AS1 NUS1P3 LINC00566 TNFRSF19 C1QTNF9 SPATA13
nsv832566 Chr.13:23849425 - 24011494 on Build GRCh38 Gain C1QTNF9B-AS1 ANKRD20A19P C1QTNF9B MIPEP SPATA13
esv3892311 Chr.13:22674660 - 24411768 on Build GRCh38 Gain C1QTNF9B-AS1 ANKRD20A19P LOC105370109 C1QTNF9B MIPEP SPATA13-AS1 MIR2276 LINC00327 SGCG SACS SACS-AS1 BASP1P1 NUS1P3 LINC00566 LINC00621 TNFRSF19 C1QTNF9 SPATA13
dgv1615n100 Chr.13:22930769 - 24362849 on Build GRCh38 Gain C1QTNF9B-AS1 ANKRD20A19P C1QTNF9B MIPEP SPATA13-AS1 MIR2276 LINC00327 SGCG SACS SACS-AS1 NUS1P3 LINC00566 TNFRSF19 C1QTNF9 SPATA13
esv3631536 Chr.13:23873928 - 23994831 on Build GRCh38 Gain C1QTNF9B-AS1 ANKRD20A19P C1QTNF9B MIPEP SPATA13
esv2751136 Chr.13:22982261 - 24393377 on Build GRCh38 Loss C1QTNF9B-AS1 ANKRD20A19P C1QTNF9B MIPEP SPATA13-AS1 MIR2276 LINC00327 SGCG SACS SACS-AS1 NUS1P3 LINC00566 TNFRSF19 C1QTNF9 SPATA13
esv3580576 Chr.13:22945778 - 24362710 on Build GRCh38 Loss C1QTNF9B-AS1 ANKRD20A19P C1QTNF9B MIPEP SPATA13-AS1 MIR2276 LINC00327 SGCG SACS SACS-AS1 NUS1P3 LINC00566 TNFRSF19 C1QTNF9 SPATA13
nsv518839 Chr.13:23908914 - 23941023 on Build GRCh38 Loss ANKRD20A19P
esv2422502 Chr.13:22755560 - 24382791 on Build GRCh38 Duplication C1QTNF9B-AS1 ANKRD20A19P LOC105370109 C1QTNF9B MIPEP SPATA13-AS1 MIR2276 LINC00327 SGCG SACS SACS-AS1 BASP1P1 NUS1P3 LINC00566 LINC00621 TNFRSF19 C1QTNF9 SPATA13

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More Information


Additional Information:

For this assay, SNP(s) [rs79883960] 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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