Genomic variant #0000442538

Individual ID 00210053
Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification -
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_40447587)_(40509154_?)del
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr2_009510
Variant remarks -
Reference PubMed: Vadgama 2019, Journal: Vadgama 2019
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Nirmal Vadgama
Options




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Technique     

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Genes screened     

Variants found     

Owner     
0000211111 DNA arrayCNV Blood Microarray - 1 Nirmal Vadgama