Resource
| Id | hg38/variant_frequencies/gnomAD_4.1.0/exomes/sas |
|---|---|
| Type | allele_score |
| Version | 0 |
| Summary | gnomAD v4.1.0 exome variants (South Asian) |
| 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, 8.63e+04] |
|
| AN | int |
- |
Total number of alleles
|
 |
[1, 8.63e+04] |
|
| AF | float |
gnomad_v4_exome_sas_af |
Alternate allele frequency
|
 |
[1.16e-05, 1] |
|
| AF_percent | float |
- |
Alternate allele frequency as percent
|
 |
[0.00116, 100] |
|
n counts alleles; sd is the population standard deviation.
Alleles
| Chromosome | Alleles | substitution % | insertion % | deletion % | complex % | other % |
|---|---|---|---|---|---|---|
| all chromosomes | 16011715 | 89.78% | 4.04% | 6.18% | <0.01% | 0.00% |
| chr1 | 1574569 | 90.21% | 3.80% | 5.99% | <0.01% | 0.00% |
| chr2 | 1143139 | 89.82% | 3.94% | 6.24% | 0.00% | 0.00% |
| chr3 | 887145 | 89.71% | 4.01% | 6.28% | <0.01% | 0.00% |
| chr4 | 624612 | 89.43% | 4.04% | 6.52% | 0.00% | 0.00% |
| chr5 | 692943 | 89.49% | 4.11% | 6.40% | 0.00% | 0.00% |
| chr6 | 753704 | 89.29% | 4.22% | 6.49% | 0.00% | 0.00% |
| chr7 | 834475 | 89.56% | 4.13% | 6.32% | <0.01% | 0.00% |
| chr8 | 584606 | 90.30% | 3.77% | 5.93% | 0.00% | 0.00% |
| chr9 | 691367 | 90.05% | 4.05% | 5.91% | 0.00% | 0.00% |
| chr10 | 642166 | 89.91% | 3.93% | 6.16% | 0.00% | 0.00% |
| chr11 | 927667 | 90.27% | 3.90% | 5.83% | 0.00% | 0.00% |
| chr12 | 831726 | 89.14% | 4.28% | 6.58% | <0.01% | 0.00% |
| chr13 | 289160 | 88.87% | 4.31% | 6.82% | 0.00% | 0.00% |
| chr14 | 530442 | 89.60% | 4.04% | 6.36% | 0.00% | 0.00% |
| chr15 | 615899 | 90.04% | 3.86% | 6.10% | <0.01% | 0.00% |
| chr16 | 810474 | 90.67% | 3.70% | 5.64% | 0.00% | 0.00% |
| chr17 | 938841 | 89.58% | 4.21% | 6.21% | 0.00% | 0.00% |
| chr18 | 245749 | 89.29% | 4.24% | 6.47% | 0.00% | 0.00% |
| chr19 | 1056719 | 89.26% | 4.44% | 6.30% | 0.00% | 0.00% |
| chr20 | 392788 | 89.66% | 4.33% | 6.01% | <0.01% | 0.00% |
| chr21 | 187125 | 89.39% | 4.10% | 6.51% | 0.00% | 0.00% |
| chr22 | 406689 | 90.30% | 3.95% | 5.75% | <0.01% | 0.00% |
| chrX | 338950 | 89.85% | 4.04% | 6.11% | 0.00% | 0.00% |
| chrY | 10760 | 92.90% | 2.50% | 4.60% | 0.00% | 0.00% |
Substitution matrix
| ref → alt | A | C | G | T |
|---|---|---|---|---|
| A | 0 0.00% | 475819 3.31% | 1481583 10.31% | 371190 2.58% |
| C | 1189877 8.28% | 0 0.00% | 743819 5.17% | 2980229 20.73% |
| G | 2989912 20.80% | 743908 5.17% | 0 0.00% | 1067256 7.42% |
| T | 371701 2.59% | 1482652 10.31% | 477336 3.32% | 0 0.00% |
ts/tv
1.64
8,934,376 transitions
/ 5,440,906 transversions
Indel lengths
| alleles | min | max | mean | median | |
|---|---|---|---|---|---|
| insertions | 646564 | 1 | 501 | 7.67 | 2 |
| deletions | 989862 | 1 | 294 | 5.53 | 2 |
×
×
Complex alleles
| reference length | alternative length | alleles | % of complex |
|---|---|---|---|
| ≥64 | 1 | 7 | 100.00% |
Files
| Filename | Size | md5 |
|---|---|---|
| genomic_resource.yaml | 2.37 KB | a77a51a87363b4ed1dc301efe7fc2fff |
| gnomad_4_1_0_exomes_sas_data.txt.bgz | 276.35 MB | 13e836bc531b36db4be0ddf988978af3 |
| gnomad_4_1_0_exomes_sas_data.txt.bgz.tbi | 761.73 KB | afe1dcea5dbe2dba2b2b04916a705d7c |
| statistics/ |