Variant #0000880115 (NC_000006.11:g.(?_264755)_(346084_?)del)

Individual ID 00324889
Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_264755)_(346084_?)del
DNA change (hg38) -
Published as del 6p25.3 (264,755-346,084)
ISCN -
DB-ID chr6_007457
Variant remarks 81kb deletion
Reference PubMed: Schalk 2022
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 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-10-03 11:15:01 +02:00 (CEST)
Date last edited 2022-11-28 12:33:12 +01:00 (CET)
Options




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000326096 DNA SEQ;SEQ-NG - - EIF2C1 2 Johan den Dunnen


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.