Variant CNV_M1_HG19_13_20289411_20299878
Location: chr13:20289411-20299878 (10Kb)
Site classification: Multi-allelic
Variant DCN frequency: 0.002
Genes Overlapped
Site classification: Multi-allelic
Variant DCN frequency: 0.002
Genes Overlapped
PSPC1 | INTRON | paraspeckle component 1 |
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 69 0 LWK 0 1 68 0 MXL 0 0 54 0 PUR 0 0 51 1 TSI 0 0 83 0 YRI 0 0 71 0 AFR 0 1 139 0 AFR+ 0 1 184 0 AMR 0 0 154 1 ASN 0 0 238 0 EUR 0 0 271 0 ALL 0 1 847 1
Diploid copy number distribution (95% confident)
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 69 0 LWK 0 1 68 0 MXL 0 0 54 0 PUR 0 0 51 1 TSI 0 0 83 0 YRI 0 0 71 0 AFR 0 1 139 0 AFR+ 0 1 184 0 AMR 0 0 154 1 ASN 0 0 238 0 EUR 0 0 271 0 ALL 0 1 847 1
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI