Genomic variant #0000665688

Individual ID 00050103
Chromosome Y
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification -
DNA change (genomic) (Relative to hg19 / GRCh37) g.[NC_000003.11:pter_77220642]delinspter_4892525
DNA change (hg38) -
Published as -
ISCN 46,XY,t(Y;3)(p11;p12)dn
DB-ID chrY_000000 See all 4 reported entries
Variant remarks transcript not studied
Reference -
ClinVar ID -
dbSNP ID -
Origin DUPLICATE record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Genomic location of variant could not be determined
Owner Johan den Dunnen




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000050045 DNA;RNA FISH;PCR;RT-PCR;SEQ - - PCDH11Y, ROBO2 5 Johan den Dunnen