Variant #0000351629 (NC_000004.11:g.(823367_851095)_(14858637_14889403)del)

Individual ID 00151937
Chromosome 4
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.(823367_851095)_(14858637_14889403)del
DNA change (hg38) -
Published as -
ISCN del(4)(p15.32p16.3)
DB-ID chr4_003281
Variant remarks 13.63 Mb isolated interstitial deletion
Reference PubMed: Shimizu 2014
ClinVar ID -
dbSNP ID -
Origin De novo
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 2018-01-28 09:38:22 +01:00 (CET)
Date last edited 2019-03-01 23:23:53 +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     
0000152794 DNA arrayCGH;FISH - - WHSC1 1 Johan den Dunnen


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