Variant CNV_M1_HG19_2_3732694_3737637
Location: chr2:3732694-3737637 (4.9Kb)
Site classification: Deletion
Variant DCN frequency: 0.105
Genes Overlapped
Site classification: Deletion
Variant DCN frequency: 0.105
Genes Overlapped
| ALLC | INTRON | probable allantoicase |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2
ASW 0 0 45
CEU 1 8 57
CHB 2 16 60
CHS 1 20 70
CLM 0 4 45
FIN 0 6 56
GBR 0 3 51
IBS 0 2 4
JPT 0 10 59
LWK 0 0 69
MXL 0 6 48
PUR 0 3 49
TSI 0 8 75
YRI 0 0 71
AFR 0 0 140
AFR+ 0 0 185
AMR 0 13 142
ASN 3 46 189
EUR 1 27 243
ALL 4 86 759
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2
ASW 0 0 45
CEU 1 8 57
CHB 2 16 60
CHS 1 20 70
CLM 0 3 45
FIN 0 6 56
GBR 0 3 51
IBS 0 2 4
JPT 0 10 59
LWK 0 0 69
MXL 0 6 48
PUR 0 3 49
TSI 0 8 75
YRI 0 0 71
AFR 0 0 140
AFR+ 0 0 185
AMR 0 12 142
ASN 3 46 189
EUR 1 27 243
ALL 4 85 759
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI