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See other DEFB119 CNV Assays ›
Gene Symbol
DEFB119
Assay Reference Genome
Location

Chr.20:31386112 on build GRCh38
Cytoband
20q11.21
Assay ID Hs04042777_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 245932

Gene Name:

 defensin beta 119

Gene Aliases:

 DEFB-19, DEFB-20, DEFB120, DEFB20, ESC42-RELA, ESC42-RELB

Location:

 Chr.20:31377163-31390649 on Build GRCh38

Assay Gene Location:

 Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
DEFB119 NM_153289.3 NP_695021.2
NR_073151.1
NR_073152.1
NR_073153.1
NR_126440.1
AF479698.1 AAQ05837.1
AL732301.1
AW003815.1
AY122472.1 AAM93914.1
AY358860.1 AAQ89219.1
AY501001.1 AAS87295.1
BC062212.1 AAH62212.1
BI460707.1
BU561156.1
HY035342.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv470546 Chr.20:31245806 - 31647499 on Build GRCh38 Gain COX4I2 REM1 LINC00028 DEFB117 DEFB122 DEFB115 DEFB123 DEFB118 DEFB116 ID1 HM13 LOC107985416 MIR3193 DEFB121 HM13-AS1 DEFB119 DEFB124
nsv1060041 Chr.20:31339025 - 31428640 on Build GRCh38 Gain DEFB117 DEFB121 DEFB122 DEFB118 DEFB119
esv2763228 Chr.20:31247246 - 31651719 on Build GRCh38 Gain COX4I2 REM1 LINC00028 DEFB117 DEFB122 DEFB115 DEFB123 DEFB118 DEFB116 ID1 HM13 LOC107985416 MIR3193 DEFB121 HM13-AS1 DEFB119 DEFB124
dgv4299n100 Chr.20:31247234 - 31436365 on Build GRCh38 Gain DEFB117 DEFB121 DEFB122 DEFB115 DEFB118 DEFB116 DEFB119
esv3645647 Chr.20:31367312 - 31405042 on Build GRCh38 Gain DEFB121 DEFB118 DEFB119
nsv585910 Chr.20:31305698 - 31457590 on Build GRCh38 Gain DEFB117 DEFB121 DEFB122 DEFB123 DEFB118 DEFB116 DEFB119
esv3645644 Chr.20:31257358 - 31413171 on Build GRCh38 Loss DEFB117 DEFB121 DEFB115 DEFB118 DEFB116 DEFB119

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More Information


Additional Information:

For this assay, SNP(s) [rs114442976] 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

Panther Classification:

Gene Ontology Categories:

Function(s)


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