Resource
| Id | hg38/variant_frequencies/gnomAD_4.1.0/exomes/nfe |
|---|---|
| Type | allele_score |
| Version | 0 |
| Summary | gnomAD v4.1.0 exome variants (Non-Finnish European) |
| Description |
gnomAD, or the Genome Aggregation Database, is a comprehensive resource of human genetic variation, managed by the Broad Institute of MIT and Harvard. It aggregates data from numerous genomic studies, compiling information on millions of genetic variants from the genomes and exomes of hundreds of thousands of individuals. This extensive database aids genetic research, enhancing our understanding of the genetic basis of diseases and supporting the development of precision medicine by providing insights into the distribution of genetic variations across diverse populations. Downloaded on 6/27/2024 https://gnomad.broadinstitute.org/downloads |
| Labels |
|
Scores (4)
| ID | Type | Default annotation | Description | Histogram | Range | Summary |
|---|---|---|---|---|---|---|
| AC | int |
- |
Alternate allele count
|
 |
[1, 1.11e+06] |
|
| AN | int |
- |
Total number of alleles
|
 |
[1, 1.11e+06] |
|
| AF | float |
gnomad_v4_exome_nfe_af |
Alternate allele frequency
|
 |
[8.99e-07, 1] |
|
| AF_percent | float |
- |
Alternate allele frequency as percent
|
 |
[8.99e-05, 100] |
|
n counts alleles; sd is the population standard deviation.
Alleles
| Chromosome | Alleles | substitution % | insertion % | deletion % | complex % | other % |
|---|---|---|---|---|---|---|
| all chromosomes | 51581751 | 89.96% | 3.69% | 6.35% | <0.01% | 0.00% |
| chr1 | 5090020 | 90.22% | 3.52% | 6.26% | <0.01% | 0.00% |
| chr2 | 3753656 | 90.03% | 3.58% | 6.39% | 0.00% | 0.00% |
| chr3 | 2911006 | 89.97% | 3.59% | 6.43% | <0.01% | 0.00% |
| chr4 | 2041503 | 89.84% | 3.58% | 6.57% | <0.01% | 0.00% |
| chr5 | 2271149 | 89.85% | 3.68% | 6.47% | 0.00% | 0.00% |
| chr6 | 2471139 | 89.85% | 3.65% | 6.51% | 0.00% | 0.00% |
| chr7 | 2615026 | 89.82% | 3.74% | 6.44% | <0.01% | 0.00% |
| chr8 | 1874295 | 90.39% | 3.48% | 6.13% | <0.01% | 0.00% |
| chr9 | 2210360 | 90.11% | 3.75% | 6.14% | 0.00% | 0.00% |
| chr10 | 2078399 | 90.11% | 3.54% | 6.35% | 0.00% | 0.00% |
| chr11 | 2986576 | 90.29% | 3.62% | 6.09% | <0.01% | 0.00% |
| chr12 | 2701206 | 89.61% | 3.78% | 6.61% | 0.00% | 0.00% |
| chr13 | 938661 | 89.44% | 3.71% | 6.85% | <0.01% | 0.00% |
| chr14 | 1698910 | 89.68% | 3.79% | 6.53% | 0.00% | 0.00% |
| chr15 | 1935286 | 90.10% | 3.56% | 6.35% | <0.01% | 0.00% |
| chr16 | 2522799 | 90.60% | 3.51% | 5.89% | <0.01% | 0.00% |
| chr17 | 3006283 | 89.71% | 3.91% | 6.38% | 0.00% | 0.00% |
| chr18 | 812370 | 89.56% | 3.79% | 6.65% | 0.00% | 0.00% |
| chr19 | 3331256 | 89.41% | 4.14% | 6.45% | 0.00% | 0.00% |
| chr20 | 1260413 | 89.75% | 3.99% | 6.26% | <0.01% | 0.00% |
| chr21 | 570700 | 89.33% | 3.97% | 6.71% | 0.00% | 0.00% |
| chr22 | 1255400 | 90.05% | 3.83% | 6.11% | <0.01% | 0.00% |
| chrX | 1212507 | 90.47% | 3.55% | 5.98% | 0.00% | 0.00% |
| chrY | 32831 | 92.78% | 2.32% | 4.90% | 0.00% | 0.00% |
Substitution matrix
| ref → alt | A | C | G | T |
|---|---|---|---|---|
| A | 0 0.00% | 1871956 4.03% | 5112186 11.02% | 1521541 3.28% |
| C | 3791849 8.17% | 0 0.00% | 2756826 5.94% | 8254011 17.79% |
| G | 8277497 17.84% | 2750921 5.93% | 0 0.00% | 3547711 7.65% |
| T | 1528070 3.29% | 5113383 11.02% | 1878731 4.05% | 0 0.00% |
ts/tv
1.36
26,757,077 transitions
/ 19,647,605 transversions
Indel lengths
| alleles | min | max | mean | median | |
|---|---|---|---|---|---|
| insertions | 1902292 | 1 | 567 | 8.42 | 2 |
| deletions | 3274756 | 1 | 344 | 5.16 | 2 |
×
×
Complex alleles
| reference length | alternative length | alleles | % of complex |
|---|---|---|---|
| ≥64 | 1 | 21 | 100.00% |
Files
| Filename | Size | md5 |
|---|---|---|
| genomic_resource.yaml | 2.38 KB | e044fe574de16326192b3d68484d0add |
| gnomad_4_1_0_exomes_nfe_data.txt.bgz | 915.56 MB | 56269709bb5458333228b64812971b62 |
| gnomad_4_1_0_exomes_nfe_data.txt.bgz.tbi | 980.21 KB | 7caabafeb4aeb78dc29a0a99d90d4caf |
| statistics/ |