Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target Variation ID |
Location |
CNV Subtype |
Genes |
nsv1057847 |
Chr20:42652464 - 44431352 on Build GRCh38 |
Loss |
TOX2
LOC105372626
MYBL2
HNF4A-AS1
MIR3646
OSER1-AS1
PTPRT
FITM2
LOC101927138
GDAP1L1
JPH2
LOC101927200
R3HDML
HNF4A
SRSF6
IFT52
SGK2
L3MBTL1
LOC101927159
GTSF1L
OSER1
|
nsv586065 |
Chr20:44261867 - 44505244 on Build GRCh38 |
Gain |
SERINC3
FITM2
GDAP1L1
LINC01620
R3HDML
HNF4A
HNF4A-AS1
MIR3646
LINC01430
TTPAL
|
Product Details
- Assay Reference Genome
Location
Chr.20:44390484 on build GRCh38
- Cytoband
- 20q13.12
- Species
- Homo sapiens
- Variation Type
- Copy Number
Additional Information
Target Gene Details
- Entrez Gene ID
- 3172
- Gene Symbol
- HNF4A
- Gene Name
- hepatocyte nuclear factor 4 alpha
- Gene Aliases
- FRTS4, HNF4, HNF4a7, HNF4a8, HNF4a9, HNF4alpha, MODY, MODY1, NR2A1, NR2A21, TCF, TCF14
- Location
- Chr.20:44355801-44432845 on build GRCh38
- Assay Gene Location
- Overlaps Intron 1 - Exon 2
- Entrez Gene ID
- 101927219
- Gene Symbol
- HNF4A-AS1
- Gene Name
- HNF4A antisense RNA 1
- Gene Aliases
- uc002xlx
- Location
- Chr.20:44377743-44395706 on build GRCh38
- Assay Gene Location
- Within Intron 2
Gene Symbol |
Transcript Accession |
Exon Location |
Assay Location |
Protein ID |
HNF4A-AS1 |
NR_109949.1 |
|
|
|
AF143870.1 |
|
|
|
Target Copy Number Variation Details
- DGV Version
- Release date: 2016-05-15, GRCh GRCh38
Target Variation |
Location |
CNV Subtype |
Genes |
nsv1057847 |
Chr20:42652464 - 44431352 on Build GRCh38 |
Loss |
TOX2
LOC105372626
MYBL2
HNF4A-AS1
MIR3646
OSER1-AS1
PTPRT
FITM2
LOC101927138
GDAP1L1
JPH2
LOC101927200
R3HDML
HNF4A
SRSF6
IFT52
SGK2
L3MBTL1
LOC101927159
GTSF1L
OSER1
|
nsv586065 |
Chr20:44261867 - 44505244 on Build GRCh38 |
Gain |
SERINC3
FITM2
GDAP1L1
LINC01620
R3HDML
HNF4A
HNF4A-AS1
MIR3646
LINC01430
TTPAL
|
View Full Product Details