Variant CNV_M1_HG19_12_8894733_8898798
Location: chr12:8894733-8898798 (4.1Kb)
Site classification: Deletion
Variant DCN frequency: 0.017
Genes Overlapped
Site classification: Deletion
Variant DCN frequency: 0.017
Genes Overlapped
| RIMKLB | INTRON | ribosomal modification protein rimK-like family member B |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2
ASW 0 3 42
CEU 0 0 66
CHB 0 0 78
CHS 0 0 91
CLM 0 0 49
FIN 0 0 62
GBR 0 0 54
IBS 0 0 6
JPT 0 0 69
LWK 1 4 64
MXL 0 0 54
PUR 0 2 50
TSI 0 0 83
YRI 0 5 66
AFR 1 9 130
AFR+ 1 12 172
AMR 0 2 153
ASN 0 0 238
EUR 0 0 271
ALL 1 14 834
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2
ASW 0 2 42
CEU 0 0 66
CHB 0 0 78
CHS 0 0 91
CLM 0 0 49
FIN 0 0 62
GBR 0 0 54
IBS 0 0 6
JPT 0 0 69
LWK 1 4 63
MXL 0 0 54
PUR 0 2 50
TSI 0 0 83
YRI 0 5 66
AFR 1 9 129
AFR+ 1 11 171
AMR 0 2 153
ASN 0 0 238
EUR 0 0 271
ALL 1 13 833
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI