Variant #0000785361 (NC_000019.9:g.(42580845_42632535)_(42947378_43001360)del)

Individual ID 00373335
Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(42580845_42632535)_(42947378_43001360)del
DNA change (hg38) -
Published as -
ISCN arr[hg19] 19q13.2(42632535_42947378)×1 dn
DB-ID chr19_006594
Variant remarks Maximum size: 420.5 kb, g.42580845_43001360del
Reference Singh R and Cohen ASA, et al. Cold Spring Harb Mol Case Stud, 2021.
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Stuart Scott
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Stuart Scott
Date created 2021-05-13 18:07:11 +02:00 (CEST)
Date last edited 2021-05-17 09:02:56 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000374570 DNA arrayCGH - Agilent 4x180K - 1 Stuart Scott


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