Variant CNV_M1_HG19_15_33906588_33910718
Location: chr15:33906588-33910718 (4.1Kb)
Site classification: Deletion
Variant DCN frequency: 0.009
Genes Overlapped
Site classification: Deletion
Variant DCN frequency: 0.009
Genes Overlapped
| RYR3 | INTRON | ryanodine receptor 3 isoform 2 |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2 CN3
ASW 0 0 45 0
CEU 0 0 66 0
CHB 0 3 75 0
CHS 0 1 90 0
CLM 0 0 49 0
FIN 0 0 62 0
GBR 0 0 54 0
IBS 0 0 6 0
JPT 0 4 65 0
LWK 0 0 69 0
MXL 0 0 53 1
PUR 0 0 52 0
TSI 0 0 83 0
YRI 0 0 71 0
AFR 0 0 140 0
AFR+ 0 0 185 0
AMR 0 0 154 1
ASN 0 8 230 0
EUR 0 0 271 0
ALL 0 8 840 1
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2
ASW 0 0 45
CEU 0 0 66
CHB 0 3 75
CHS 0 1 90
CLM 0 0 49
FIN 0 0 62
GBR 0 0 54
IBS 0 0 6
JPT 0 4 65
LWK 0 0 69
MXL 0 0 53
PUR 0 0 52
TSI 0 0 83
YRI 0 0 71
AFR 0 0 140
AFR+ 0 0 185
AMR 0 0 154
ASN 0 8 230
EUR 0 0 271
ALL 0 8 840
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI