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120 changes: 60 additions & 60 deletions
120
browser/src/MitochondrialVariantPage/__snapshots__/MitochondrialVariantPage.spec.tsx.snap
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12 changes: 12 additions & 0 deletions
12
browser/src/StatsPage/BarGraphData/gnomADExomeGenomeCountsByVersion.json
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{ | ||
"colors": { | ||
"Exomes": "#0e6fbf", | ||
"Genomes": "#508a14" | ||
}, | ||
"data": [ | ||
{ "label": "ExAC", "Exomes": 60706, "Genomes": 0 }, | ||
{ "label": "gnomAD v2", "Exomes": 125758, "Genomes": 15708 }, | ||
{ "label": "gnomAD v3", "Exomes": 0, "Genomes": 76156 }, | ||
{ "label": "gnomAD v4", "Exomes": 730947, "Genomes": 76215 } | ||
] | ||
} |
59 changes: 59 additions & 0 deletions
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browser/src/StatsPage/BarGraphData/gnomadV4GeneticAncestryCounts.json
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{ | ||
"colors": { | ||
"East Asian": "#0e8b45", | ||
"South Asian": "#ff9a10", | ||
"Middle Eastern": "#050080", | ||
"African": "#931193", | ||
"Admixed American": "#ed1e23", | ||
"Ashkenazi Jewish": "#edc800", | ||
"European": "#6aa5ce", | ||
"Remaining": "#acb8b9" | ||
}, | ||
"data": [ | ||
{ | ||
"label": "ExAC", | ||
"East Asian": 4327, | ||
"South Asian": 8256, | ||
"Middle Eastern": 0, | ||
"African": 5203, | ||
"Admixed American": 5789, | ||
"Ashkenazi Jewish": 0, | ||
"Remaining": 454, | ||
"European": 36677 | ||
}, | ||
{ | ||
"label": "gnomAD v2", | ||
"East Asian": 9977, | ||
"South Asian": 15308, | ||
"Middle Eastern": 0, | ||
"African": 12487, | ||
"Admixed American": 17720, | ||
"Ashkenazi Jewish": 5185, | ||
"Remaining": 3614, | ||
"European": 77165 | ||
}, | ||
{ | ||
"label": "gnomAD v3", | ||
"East Asian": 2604, | ||
"South Asian": 2419, | ||
"Middle Eastern": 158, | ||
"African": 20744, | ||
"Admixed American": 7647, | ||
"Ashkenazi Jewish": 1736, | ||
"Remaining": 1503, | ||
"European": 39345 | ||
}, | ||
|
||
{ | ||
"label": "gnomAD v4", | ||
"East Asian": 19850, | ||
"South Asian": 43129, | ||
"Middle Eastern": 2884, | ||
"African": 16740, | ||
"Admixed American": 22362, | ||
"Ashkenazi Jewish": 13068, | ||
"Remaining": 30198, | ||
"European": 582716 | ||
} | ||
] | ||
} |
36 changes: 36 additions & 0 deletions
36
browser/src/StatsPage/BarGraphData/gnomadV4GeneticDiversityCounts.json
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{ | ||
"colors": { | ||
"East Asian": "#0e8b45", | ||
"South Asian": "#ff9a10", | ||
"European": "#6aa5ce", | ||
"Middle Eastern": "#050080", | ||
"African": "#931193", | ||
"Admixed American": "#ed1e23", | ||
"Ashkenazi Jewish": "#edc800", | ||
"Remaining": "#acb8b9" | ||
}, | ||
"data": [ | ||
{ | ||
"label": "gnomAD v2", | ||
"East Asian": 600, | ||
"South Asian": 750, | ||
"European": 450, | ||
"Middle Eastern": 0, | ||
"African": 1350, | ||
"Admixed American": 750, | ||
"Ashkenazi Jewish": 350, | ||
"Remaining": 1500 | ||
}, | ||
{ | ||
"label": "gnomAD v4", | ||
"East Asian": 2000, | ||
"South Asian": 3000, | ||
"European": 2000, | ||
"Middle Eastern": 3000, | ||
"African": 4000, | ||
"Admixed American": 3500, | ||
"Ashkenazi Jewish": 1150, | ||
"Remaining": 3500 | ||
} | ||
] | ||
} |
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import React from 'react' | ||
import styled from 'styled-components' | ||
|
||
const Container = styled.div` | ||
margin-left: 2rem; | ||
` | ||
|
||
const Section = styled.div` | ||
margin-bottom: 1em; | ||
` | ||
|
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const SectionHeader = styled.div` | ||
font-size: 1.1em; | ||
font-weight: bold; | ||
` | ||
|
||
const SectionList = styled.ul` | ||
margin-top: 0.5em; | ||
li { | ||
margin-bottom: 0.5em; | ||
} | ||
` | ||
|
||
const NumberOfVariantsInGnomadList = () => { | ||
return ( | ||
<Container> | ||
<Section> | ||
<SectionHeader>Short variants</SectionHeader> | ||
<SectionList> | ||
<li>Total SNVs: 786,500,648</li> | ||
<li>Total InDels: 122,583,462</li> | ||
<li> | ||
Variant type totals | ||
<SectionList> | ||
<li>Synonymous: 9,643,254</li> | ||
<li>Missense: 16,412,219</li> | ||
<li>Nonsense: 726,924</li> | ||
<li>Frameshift: 1,186,588</li> | ||
<li>Canonical splice site: 542,514</li> | ||
</SectionList> | ||
</li> | ||
</SectionList> | ||
</Section> | ||
<Section> | ||
<SectionHeader>Structural variants</SectionHeader> | ||
<SectionList> | ||
<li> | ||
1,199,106 genome SVs | ||
<SectionList> | ||
<li>627,942 Depletions</li> | ||
<li>258,876 Duplications</li> | ||
<li>711 CNVs</li> | ||
<li>296,184 Insertions</li> | ||
<li>2,185 Inversersions</li> | ||
<li>13,116 Complex</li> | ||
<li>92 Canonical recriprocal translocations</li> | ||
</SectionList> | ||
</li> | ||
<li> | ||
{`66,826 rare (<1% AF) exome CNVs`} | ||
<SectionList> | ||
<li>30,855 Deletions</li> | ||
<li>35,971 Duplications</li> | ||
</SectionList> | ||
</li> | ||
</SectionList> | ||
</Section> | ||
<Section> | ||
<SectionHeader>Average number of variants per person</SectionHeader> | ||
<SectionList> | ||
<li> | ||
SNVs per person (<i>coming soon</i>) | ||
<SectionList> | ||
<li>On average we see 2 SNVs every 3 base pairs</li> | ||
</SectionList> | ||
</li> | ||
<li>{`1 rare (<1% AF) coding CNV per individual`}</li> | ||
<li>11,844 SVs per genome</li> | ||
</SectionList> | ||
</Section> | ||
</Container> | ||
) | ||
} | ||
|
||
export default NumberOfVariantsInGnomadList |
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