Variant #0000351613 (NC_000004.11:g.(pter_73075)_(2092144_2101270)del)
| Individual ID |
00151921 |
| 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.(pter_73075)_(2092144_2101270)del |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
46,XX der(4)t(4;10)(p16.3;q26.3) |
| DB-ID |
chr4_003265 |
| Variant remarks |
2.06 Mb deletion/772 kb duplication, unbalanced translocation |
| Reference |
PubMed: Shimizu 2014 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| 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 |
2019-03-03 17:38:57 +01:00 (CET) |
Variant on transcripts
Screenings
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