Variant #0000351629 (NC_000004.11:g.(823367_851095)_(14858637_14889403)del)
| Individual ID |
00151937 |
| Chromosome |
4 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(823367_851095)_(14858637_14889403)del |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
del(4)(p15.32p16.3) |
| DB-ID |
chr4_003281 |
| Variant remarks |
13.63 Mb isolated interstitial deletion |
| Reference |
PubMed: Shimizu 2014 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
De novo |
| 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 |
2018-01-28 09:38:22 +01:00 (CET) |
| Date last edited |
2019-03-01 23:23:53 +01:00 (CET) |

Variant on transcripts
Screenings
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