Variant CNV_M1_HG19_8_15419660_15440485
Location: chr8:15419660-15440485 (20Kb)
Site classification: Multi-allelic
Variant DCN frequency: 0.007
Genes Overlapped
Site classification: Multi-allelic
Variant DCN frequency: 0.007
Genes Overlapped
| TUSC3 | INTRON | tumor suppressor candidate 3 precursor |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2 CN3 CN4
ASW 0 0 45 0 0
CEU 0 0 66 0 0
CHB 0 0 77 1 0
CHS 0 0 91 0 0
CLM 0 0 49 0 0
FIN 0 0 62 0 0
GBR 0 0 53 0 1
IBS 0 0 6 0 0
JPT 0 0 69 0 0
LWK 0 1 68 0 0
MXL 0 0 54 0 0
PUR 0 0 51 1 0
TSI 0 1 81 1 0
YRI 0 0 71 0 0
AFR 0 1 139 0 0
AFR+ 0 1 184 0 0
AMR 0 0 154 1 0
ASN 0 0 237 1 0
EUR 0 1 268 1 1
ALL 0 2 843 3 1
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2 CN3 CN4
ASW 0 0 45 0 0
CEU 0 0 66 0 0
CHB 0 0 77 1 0
CHS 0 0 91 0 0
CLM 0 0 49 0 0
FIN 0 0 62 0 0
GBR 0 0 53 0 1
IBS 0 0 6 0 0
JPT 0 0 69 0 0
LWK 0 1 68 0 0
MXL 0 0 54 0 0
PUR 0 0 51 1 0
TSI 0 1 81 1 0
YRI 0 0 71 0 0
AFR 0 1 139 0 0
AFR+ 0 1 184 0 0
AMR 0 0 154 1 0
ASN 0 0 237 1 0
EUR 0 1 268 1 1
ALL 0 2 843 3 1
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI