Variant CNV_M1_HG19_1_1602244_1617450
Location: chr1:1602244-1617450 (15Kb)
Site classification: Multi-allelic
Variant DCN frequency: 0.012
Genes Overlapped
Site classification: Multi-allelic
Variant DCN frequency: 0.012
Genes Overlapped
| SLC35E2B | CDS | solute carrier family 35 member E2B |
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 0 75 3
CHS 0 0 89 2
CLM 0 0 49 0
FIN 0 1 61 0
GBR 0 0 52 2
IBS 0 0 6 0
JPT 0 0 69 0
LWK 0 2 67 0
MXL 0 0 53 1
PUR 0 0 50 2
TSI 0 0 83 0
YRI 0 0 71 0
AFR 0 2 138 0
AFR+ 0 2 183 0
AMR 0 0 152 3
ASN 0 0 233 5
EUR 0 1 268 2
ALL 0 3 836 10
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2 CN3
ASW 0 0 44 0
CEU 0 0 65 0
CHB 0 0 75 3
CHS 0 0 87 0
CLM 0 0 46 0
FIN 0 0 61 0
GBR 0 0 51 2
IBS 0 0 6 0
JPT 0 0 69 0
LWK 0 2 67 0
MXL 0 0 53 1
PUR 0 0 50 2
TSI 0 0 83 0
YRI 0 0 71 0
AFR 0 2 138 0
AFR+ 0 2 182 0
AMR 0 0 149 3
ASN 0 0 231 3
EUR 0 0 266 2
ALL 0 2 828 8
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI