Variant #0000129140 (NC_000011.9:g.(pter_196966)_(7001800_10700000)dup)
| Individual ID |
00080104 |
| Chromosome |
11 |
| 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.(pter_196966)_(7001800_10700000)dup |
| DNA change (hg38) |
- |
| Published as |
arr[hg18] 11p15.5-p15.4(186,966-6,958,376)x3 mat |
| ISCN |
arr[hg19] 11p15.5-p15.4(196,966-7,001,800)x3 mat |
| DB-ID |
chr11_000459 |
| Variant remarks |
duplication |
| Reference |
PubMed: Cardarelli 2010, PubMed: Fokstuen 2013, for EUCID-SRS consortium |
| 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 |
Zeynep Tümer |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2016-09-01 17:30:25 +02:00 (CEST) |
| Date last edited |
2020-10-01 16:53:33 +02:00 (CEST) |
Variant on transcripts
Screenings
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