Variant #0000785361 (NC_000019.9:g.(42580845_42632535)_(42947378_43001360)del)
| Individual ID |
00373335 |
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(42580845_42632535)_(42947378_43001360)del |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
arr[hg19] 19q13.2(42632535_42947378)×1 dn |
| DB-ID |
chr19_006594 |
| Variant remarks |
Maximum size: 420.5 kb, g.42580845_43001360del |
| Reference |
Singh R and Cohen ASA, et al. Cold Spring Harb Mol Case Stud, 2021. |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Stuart Scott |
| Database submission license |
Creative Commons Attribution-NonCommercial 4.0 International |
| Created by |
Stuart Scott |
| Date created |
2021-05-13 18:07:11 +02:00 (CEST) |
| Date last edited |
2021-05-17 09:02:56 +02:00 (CEST) |

Variant on transcripts
Screenings
|