Variant #0000404985 (NC_000023.10:g.(103160000_103174264)_(103356460_103360000)[2])
Individual ID |
00180302 |
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.(103160000_103174264)_(103356460_103360000)[2] |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
hg19 arr(103174264–103356460)x2 |
DB-ID |
chrX_010577 |
Variant remarks |
182 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 16:47:24 +02:00 (CEST) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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