Variant #0000877891 (NC_000022.10:g.(?_18656495)_(20306993_?)del)

Individual ID 00045130
Chromosome 22
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_18656495)_(20306993_?)del
DNA change (hg38) -
Published as del 18656495-20306993, genome build not mentioned
ISCN -
DB-ID chr22_003033
Variant remarks 1.6-Mb microdeletion in the Di George/VCFS region of the 22q11.2 locus
Reference PubMed: Gunes 2018
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation ?
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anna Tracewska
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-09-08 14:02:08 +02:00 (CEST)
Date last edited 2022-09-08 15:33:46 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000418141 DNA arrayCNV;FISH - - - 1 Anna Tracewska


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