Variant #0000880115 (NC_000006.11:g.(?_264755)_(346084_?)del)
| Individual ID |
00324889 |
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_264755)_(346084_?)del |
| DNA change (hg38) |
- |
| Published as |
del 6p25.3 (264,755-346,084) |
| ISCN |
- |
| DB-ID |
chr6_007457 |
| Variant remarks |
81kb deletion |
| Reference |
PubMed: Schalk 2022 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline/De novo (untested) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-10-03 11:15:01 +02:00 (CEST) |
| Date last edited |
2022-11-28 12:33:12 +01:00 (CET) |

Variant on transcripts
Screenings
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