Variant CNV_M1_HG19_13_108946897_108951674
Location: chr13:108946897-108951674 (4.8Kb)
Site classification: Deletion
Variant DCN frequency: 0.195
Genes Overlapped
Site classification: Deletion
Variant DCN frequency: 0.195
Genes Overlapped
| TNFSF13B | INTRON | tumor necrosis factor ligand superfamily member 13B |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2
ASW 1 14 30
CEU 2 17 47
CHB 0 7 71
CHS 0 4 87
CLM 0 10 39
FIN 0 12 50
GBR 2 19 33
IBS 0 0 6
JPT 0 2 67
LWK 3 20 46
MXL 0 11 43
PUR 0 2 50
TSI 1 21 61
YRI 1 20 50
AFR 4 40 96
AFR+ 5 54 126
AMR 0 23 132
ASN 0 13 225
EUR 5 69 197
ALL 10 159 680
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2
ASW 1 14 30
CEU 2 17 47
CHB 0 7 71
CHS 0 4 87
CLM 0 10 39
FIN 0 12 50
GBR 2 19 33
IBS 0 0 6
JPT 0 1 66
LWK 3 18 46
MXL 0 10 43
PUR 0 2 50
TSI 1 21 61
YRI 1 19 50
AFR 4 37 96
AFR+ 5 51 126
AMR 0 22 132
ASN 0 12 224
EUR 5 69 197
ALL 10 154 679
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI