Variant CNV_M1_HG19_8_51166298_51170837
Location: chr8:51166298-51170837 (4.5Kb)
Site classification: Multi-allelic
Variant DCN frequency: 0.004
Genes Overlapped
Site classification: Multi-allelic
Variant DCN frequency: 0.004
Genes Overlapped
| SNTG1 | INTRON | gamma-1-syntrophin |
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 1 77 0
CHS 0 0 91 0
CLM 0 0 49 0
FIN 0 0 62 0
GBR 0 0 54 0
IBS 0 0 6 0
JPT 0 0 69 0
LWK 0 0 69 0
MXL 0 1 53 0
PUR 0 0 52 0
TSI 0 0 83 0
YRI 0 0 70 1
AFR 0 0 139 1
AFR+ 0 0 184 1
AMR 0 1 154 0
ASN 0 1 237 0
EUR 0 0 271 0
ALL 0 2 846 1
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2 CN3
ASW 0 0 45 0
CEU 0 0 66 0
CHB 0 1 77 0
CHS 0 0 90 0
CLM 0 0 49 0
FIN 0 0 62 0
GBR 0 0 53 0
IBS 0 0 6 0
JPT 0 0 69 0
LWK 0 0 69 0
MXL 0 1 53 0
PUR 0 0 52 0
TSI 0 0 83 0
YRI 0 0 70 1
AFR 0 0 139 1
AFR+ 0 0 184 1
AMR 0 1 154 0
ASN 0 1 236 0
EUR 0 0 270 0
ALL 0 2 844 1
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI