Variant CNV_M1_HG19_4_77166131_77179213
Location: chr4:77166131-77179213 (13Kb)
Site classification: Deletion
Variant DCN frequency: 0.013
Genes Overlapped
Site classification: Deletion
Variant DCN frequency: 0.013
Genes Overlapped
| FAM47E | CDS | protein FAM47E isoform b |
| FAM47E-STBD1 | EXON | uncharacterized protein LOC100631383 |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2
ASW 0 0 45
CEU 0 0 66
CHB 0 0 78
CHS 0 0 91
CLM 0 0 49
FIN 0 0 62
GBR 0 0 54
IBS 0 0 6
JPT 0 0 69
LWK 1 10 58
MXL 0 0 54
PUR 0 0 52
TSI 0 0 83
YRI 0 0 71
AFR 1 10 129
AFR+ 1 10 174
AMR 0 0 155
ASN 0 0 238
EUR 0 0 271
ALL 1 10 838
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2
ASW 0 0 45
CEU 0 0 66
CHB 0 0 78
CHS 0 0 91
CLM 0 0 49
FIN 0 0 62
GBR 0 0 54
IBS 0 0 6
JPT 0 0 69
LWK 1 10 58
MXL 0 0 54
PUR 0 0 52
TSI 0 0 83
YRI 0 0 71
AFR 1 10 129
AFR+ 1 10 174
AMR 0 0 155
ASN 0 0 238
EUR 0 0 271
ALL 1 10 838
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI