Genomic variant #0000000049

Individual ID 00000001
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.792255_792256del
Reference -
DB-ID chr1_000023
dbSNP ID rs567065523
Frequency 0.003876
Allele Count 2
Allele Number 516
Combined Depth 5600
Homozygous 0
Heterozygote 2
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin