Variant CNV_M1_HG19_9_2147491_2151538
Location: chr9:2147491-2151538 (4.0Kb)
Site classification: Deletion
Variant DCN frequency: 0.025
Genes Overlapped
Site classification: Deletion
Variant DCN frequency: 0.025
Genes Overlapped
| SMARCA2 | INTRON | probable global transcription activator SNF2L2 |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2
ASW 0 1 44
CEU 1 2 63
CHB 0 0 78
CHS 0 0 91
CLM 0 0 49
FIN 1 4 57
GBR 1 4 49
IBS 0 0 6
JPT 0 0 69
LWK 0 0 69
MXL 0 1 53
PUR 0 3 49
TSI 0 5 78
YRI 0 0 71
AFR 0 0 140
AFR+ 0 1 184
AMR 0 4 151
ASN 0 0 238
EUR 3 15 253
ALL 3 20 826
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2
ASW 0 1 44
CEU 1 2 62
CHB 0 0 78
CHS 0 0 91
CLM 0 0 49
FIN 1 3 55
GBR 1 3 49
IBS 0 0 6
JPT 0 0 69
LWK 0 0 67
MXL 0 1 53
PUR 0 3 49
TSI 0 5 78
YRI 0 0 70
AFR 0 0 137
AFR+ 0 1 181
AMR 0 4 151
ASN 0 0 238
EUR 3 13 250
ALL 3 18 820
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI