Variant #0000021686 (NC_000024.9:g.(15009431_15017731)_(15592060_15603923)del)
Individual ID |
00003239 |
Chromosome |
Y |
Allele |
Paternal (inferred) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(15009431_15017731)_(15592060_15603923)del |
DNA change (hg38) |
- |
Published as |
AZFa deletion |
ISCN |
- |
DB-ID |
chrY_000092 |
Variant remarks |
AZFa deletion (sY87+, GY6_UTY1del, sY88+); undeleted father or brother |
Reference |
PubMed: Foresta 2000 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
De novo |
Segregation |
- |
Frequency |
1/92 cases |
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 |
2013-11-03 11:44:46 +01:00 (CET) |
Date last edited |
2013-11-03 13:21:35 +01:00 (CET) |

Variant on transcripts
Screenings
|