Variant CNV_M1_HG19_8_50951242_50957816
Location: chr8:50951242-50957816 (6.6Kb)
Site classification: Deletion
Variant DCN frequency: 0.001
Genes Overlapped
Site classification: Deletion
Variant DCN frequency: 0.001
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 0 78 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 0 53 1
PUR 0 0 51 1
TSI 0 0 83 0
YRI 0 1 70 0
AFR 0 1 139 0
AFR+ 0 1 184 0
AMR 0 0 153 2
ASN 0 0 238 0
EUR 0 0 271 0
ALL 0 1 846 2
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2
ASW 0 0 45
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 0 0 68
MXL 0 0 53
PUR 0 0 51
TSI 0 0 83
YRI 0 1 70
AFR 0 1 138
AFR+ 0 1 183
AMR 0 0 153
ASN 0 0 238
EUR 0 0 271
ALL 0 1 845
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI