Variant CNV_M1_HG19_2_205707172_205712081
Location: chr2:205707172-205712081 (4.9Kb)
Site classification: Multi-allelic
Variant DCN frequency: 0.005
Genes Overlapped
Site classification: Multi-allelic
Variant DCN frequency: 0.005
Genes Overlapped
| PARD3B | INTRON | partitioning defective 3 homolog B isoform a |
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 68 1
LWK 0 0 69 0
MXL 0 0 54 0
PUR 0 0 52 0
TSI 0 0 83 0
YRI 0 2 67 2
AFR 0 2 136 2
AFR+ 0 2 181 2
AMR 0 0 155 0
ASN 0 0 237 1
EUR 0 0 271 0
ALL 0 2 844 3
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2 CN3
ASW 0 0 44 0
CEU 0 0 66 0
CHB 0 0 77 0
CHS 0 0 91 0
CLM 0 0 49 0
FIN 0 0 61 0
GBR 0 0 54 0
IBS 0 0 6 0
JPT 0 0 68 0
LWK 0 0 69 0
MXL 0 0 54 0
PUR 0 0 52 0
TSI 0 0 83 0
YRI 0 2 65 2
AFR 0 2 134 2
AFR+ 0 2 178 2
AMR 0 0 155 0
ASN 0 0 236 0
EUR 0 0 270 0
ALL 0 2 839 2
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI