Variant CNV_M1_HG19_2_206113903_206121679
Location: chr2:206113903-206121679 (7.8Kb)
Site classification: Deletion
Variant DCN frequency: 0.006
Genes Overlapped
Site classification: Deletion
Variant DCN frequency: 0.006
Genes Overlapped
| PARD3B | INTRON | partitioning defective 3 homolog B isoform a |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2
ASW 0 0 45
CEU 0 1 65
CHB 0 0 78
CHS 0 0 91
CLM 0 0 49
FIN 0 0 62
GBR 0 3 51
IBS 0 0 6
JPT 0 0 69
LWK 0 0 69
MXL 0 0 54
PUR 0 0 52
TSI 0 1 82
YRI 0 0 71
AFR 0 0 140
AFR+ 0 0 185
AMR 0 0 155
ASN 0 0 238
EUR 0 5 266
ALL 0 5 844
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2
ASW 0 0 45
CEU 0 1 65
CHB 0 0 78
CHS 0 0 91
CLM 0 0 49
FIN 0 0 62
GBR 0 3 51
IBS 0 0 6
JPT 0 0 69
LWK 0 0 69
MXL 0 0 54
PUR 0 0 52
TSI 0 1 82
YRI 0 0 71
AFR 0 0 140
AFR+ 0 0 185
AMR 0 0 155
ASN 0 0 238
EUR 0 5 266
ALL 0 5 844
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI