Variant CNV_M1_HG19_18_77111773_77119003
Location: chr18:77111773-77119003 (7.2Kb)
Site classification: Duplication
Variant DCN frequency: 0.012
Genes Overlapped
Site classification: Duplication
Variant DCN frequency: 0.012
Genes Overlapped
| ATP9B | INTRON | probable phospholipid-transporting ATPase IIB |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2 CN3
ASW 0 0 41 4
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 67 2
MXL 0 0 54 0
PUR 0 0 51 1
TSI 0 0 83 0
YRI 0 0 67 4
AFR 0 0 134 6
AFR+ 0 0 175 10
AMR 0 0 154 1
ASN 0 0 237 1
EUR 0 0 271 0
ALL 0 0 837 12
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2 CN3
ASW 0 0 41 3
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 67 2
MXL 0 0 53 0
PUR 0 0 51 1
TSI 0 0 83 0
YRI 0 0 65 3
AFR 0 0 132 5
AFR+ 0 0 173 8
AMR 0 0 153 1
ASN 0 0 237 1
EUR 0 0 271 0
ALL 0 0 834 10
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI