Variant #0000351627 (NC_000004.11:g.(pter_43860)_(12397493_12435040)del)

Individual ID 00151935
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.(pter_43860)_(12397493_12435040)del
DNA change (hg38) -
Published as -
ISCN 46,XY,del(4)(p15.3p16.1)[26]/46,XY[4]
DB-ID chr4_003279
Variant remarks 12.01 Mb deletion mos.del(4)(p15.33)/del(4)(p16.3)
Reference PubMed: Shimizu 2014
ClinVar ID -
dbSNP ID -
Origin Somatic
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 2018-01-28 09:38:22 +01:00 (CET)
Date last edited 2019-03-03 17:38:57 +01:00 (CET)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000152792 DNA arrayCGH;FISH - - WHSC1 1 Johan den Dunnen


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