Variant #0000877891 (NC_000022.10:g.(?_18656495)_(20306993_?)del)
| Individual ID |
00045130 |
| Chromosome |
22 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_18656495)_(20306993_?)del |
| DNA change (hg38) |
- |
| Published as |
del 18656495-20306993, genome build not mentioned |
| ISCN |
- |
| DB-ID |
chr22_003033 |
| Variant remarks |
1.6-Mb microdeletion in the Di George/VCFS region of the 22q11.2 locus |
| Reference |
PubMed: Gunes 2018 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
De novo |
| Segregation |
? |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Anna Tracewska |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Anna Tracewska |
| Date created |
2022-09-08 14:02:08 +02:00 (CEST) |
| Date last edited |
2022-09-08 15:33:46 +02:00 (CEST) |

Variant on transcripts
Screenings
|