Variant #0000940037 (NC_000004.11:g.(?_3916090)_(4223231_?)dup)

Individual ID 00440581
Chromosome 4
Allele Paternal (confirmed)
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_3916090)_(4223231_?)dup
DNA change (hg38) -
Published as -
ISCN arr[hg19] 11p15.4(3,916,090-4,223,231)x3pat
DB-ID chr4_004641
Variant remarks -
Reference PubMed: Nil 2023
ClinVar ID -
dbSNP ID -
Origin Germline
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 2023-11-04 14:56:24 +01:00 (CET)
Date last edited N/A
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Owner     
0000442066 DNA arrayCGH;SEQ;SEQ-NG - WES - 2 Johan den Dunnen


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