Variant #0000879755 (NC_000016.9:g.(28578529_16_2883343)_(29042109_29678569)dup)

Individual ID 00418361
Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification association
DNA change (genomic) (Relative to hg19 / GRCh37) g.(28578529_16_2883343)_(29042109_29678569)dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr16_006622
Variant remarks variant not maternally inherited; associated with increased risk of being underweight and having reduced head circumference
Reference PubMed: Scott 2017
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-09-28 19:55:25 +02:00 (CEST)
Date last edited N/A




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000419656 DNA SEQ;SEQ-NG - WES - 2 Johan den Dunnen


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