Variant #0000989630 (NC_000010.10:g.(77700001_82000000)delN[(320000_460000)])
Individual ID |
00453055 |
Chromosome |
10 |
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.(77700001_82000000)delN[(320000_460000)] |
DNA change (hg38) |
g.(75900001_80300000)delN[(320000_460000)] |
Published as |
- |
ISCN |
- |
DB-ID |
chr10_005983 |
Variant remarks |
0.32-0.46 Mb 10q22.3 duplication affecting SFPTD, PLAC9 and ANXA11 |
Reference |
PubMed: Rots 2024, Journal: Rots 2024 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline/De novo (untested) |
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 |
2024-08-15 20:40:59 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
Screenings
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