Variant #0000404988 (NC_000023.10:g.(101840000_101855870)_(102556292_102570000)[2])
| Individual ID |
00180304 |
| Chromosome |
X |
| Allele |
Maternal (confirmed) |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(101840000_101855870)_(102556292_102570000)[2] |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
hg19 arr(101855870–102556292)x2 |
| DB-ID |
chrX_010580 |
| Variant remarks |
700 kb duplication |
| Reference |
PubMed: Martínez-Montero 2013, Journal: Martínez-Montero 2013 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| 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 |
2018-09-05 16:55:53 +02:00 (CEST) |
| Date last edited |
N/A |
Variant on transcripts
Screenings
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