Resource
| Id | hg38/variant_frequencies/gnomAD_4.1.0/genomes/fin |
|---|---|
| Type | allele_score |
| Version | 0 |
| Summary | gnomAD v4.1.0 genome variants (Finnish) |
| 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
|
 |
[0, 1.06e+04] |
|
| AN | int |
- |
Total number of alleles
|
 |
[0, 1.06e+04] |
|
| AF | float |
gnomad_v4_genome_fin_af |
Alternate allele frequency
|
 |
[0, 1] |
|
| AF_percent | float |
- |
Alternate allele frequency as percent
|
 |
[0, 100] |
|
n counts alleles; sd is the population standard deviation.
Alleles
| Chromosome | Alleles | substitution % | insertion % | deletion % | complex % | other % |
|---|---|---|---|---|---|---|
| all chromosomes | 459302870 | 84.92% | 7.35% | 7.73% | <0.01% | 0.00% |
| chr1 | 59160006 | 85.31% | 7.18% | 7.51% | <0.01% | 0.00% |
| chr2 | 4351620 | 75.31% | 12.03% | 12.66% | <0.01% | 0.00% |
| chr3 | 51235008 | 85.95% | 6.79% | 7.26% | <0.01% | 0.00% |
| chr4 | 3483496 | 76.05% | 11.83% | 12.12% | <0.01% | 0.00% |
| chr5 | 3178864 | 75.64% | 12.01% | 12.35% | <0.01% | 0.00% |
| chr6 | 43703160 | 85.32% | 7.18% | 7.50% | <0.01% | 0.00% |
| chr7 | 42466679 | 85.19% | 7.17% | 7.64% | <0.01% | 0.00% |
| chr8 | 2727011 | 76.65% | 11.50% | 11.85% | <0.01% | 0.00% |
| chr9 | 33833698 | 86.24% | 6.71% | 7.05% | <0.01% | 0.00% |
| chr10 | 2591683 | 74.79% | 12.37% | 12.84% | <0.01% | 0.00% |
| chr11 | 35080671 | 85.92% | 6.84% | 7.24% | <0.01% | 0.00% |
| chr12 | 2462395 | 73.85% | 12.86% | 13.29% | <0.01% | 0.00% |
| chr13 | 24993777 | 85.32% | 7.12% | 7.56% | <0.01% | 0.00% |
| chr14 | 23568672 | 85.35% | 7.11% | 7.54% | <0.01% | 0.00% |
| chr15 | 22225848 | 85.18% | 7.30% | 7.53% | <0.01% | 0.00% |
| chr16 | 1772569 | 75.33% | 12.00% | 12.67% | <0.01% | 0.00% |
| chr17 | 21944455 | 83.63% | 8.19% | 8.18% | <0.01% | 0.00% |
| chr18 | 19467717 | 85.48% | 7.02% | 7.50% | <0.01% | 0.00% |
| chr19 | 1384054 | 70.96% | 14.28% | 14.75% | <0.01% | 0.00% |
| chr20 | 16355695 | 84.43% | 7.85% | 7.72% | <0.01% | 0.00% |
| chr21 | 10958898 | 85.02% | 7.24% | 7.74% | <0.01% | 0.00% |
| chr22 | 890270 | 75.16% | 12.03% | 12.81% | <0.01% | 0.00% |
| chrX | 30297561 | 86.00% | 6.69% | 7.31% | <0.01% | 0.00% |
| chrY | 1169063 | 87.64% | 5.24% | 7.11% | 0.00% | 0.00% |
Substitution matrix
| ref → alt | A | C | G | T |
|---|---|---|---|---|
| A | 0 0.00% | 17302816 4.44% | 54069301 13.86% | 17212831 4.41% |
| C | 23555243 6.04% | 0 0.00% | 18839847 4.83% | 64119967 16.44% |
| G | 64061048 16.42% | 18827862 4.83% | 0 0.00% | 23704471 6.08% |
| T | 17095210 4.38% | 53884984 13.82% | 17351164 4.45% | 0 0.00% |
ts/tv
1.53
236,135,300 transitions
/ 153,889,444 transversions
Indel lengths
| alleles | min | max | mean | median | |
|---|---|---|---|---|---|
| insertions | 33770233 | 1 | 1381 | 14.81 | 5 |
| deletions | 35507269 | 1 | 372 | 6.84 | 2 |
×
×
Complex alleles
| reference length | alternative length | alleles | % of complex |
|---|---|---|---|
| ≥64 | 1 | 624 | 100.00% |
Files
| Filename | Size | md5 |
|---|---|---|
| genomic_resource.yaml | 2.37 KB | e0a7eb38f80194662a0b08e9bb824810 |
| gnomad_4_1_0_genomes_fin_data.txt.bgz | 2.86 GB | 34e4da9a0ddf88c6949ed6c04fd51228 |
| gnomad_4_1_0_genomes_fin_data.txt.bgz.tbi | 2.16 MB | 66ad6cf0e89a2d44c97acbee5cced3fc |
| statistics/ |