> For the complete documentation index, see [llms.txt](https://help.connected.illumina.com/llms.txt). Markdown versions of documentation pages are available by appending `.md` to page URLs; this page is available as [Markdown](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant-visualization/variant-visualization-tool/visualization-tracks/population-data-tracks.md).

# Population data tracks

These tracks help you compare case findings against internal and public population data.

## Organization DB

**\[Organization DB]** tracks display variants from [organization databases](/emedgene/emedgene-analyze-manual/settings/organization_settings_-330+/workbench-and-pipeline/organization-db-management/organization-databases.md).

Left-click a variant to review variant details from the database:

* Allele frequency
* Allele count and allele number
* Heterozygote and homozygote or hemizygote counts
* Sample IDs where the variant was last observed

## gnomAD SV

The **gnomAD SV** track displays structural variants from gnomAD.

Use it to review population frequency and distribution across diverse cohorts to support clinical relevance assessment.

<figure><img src="/files/nydt0TszkrYQdEmN8ccM" alt=""><figcaption></figcaption></figure>

## DGV Gold

The **DGV Gold** track displays high-confidence structural variants curated by the Database of Genomic Variants.

Use it as a reference for common benign structural variants.

<figure><img src="/files/Nlx1XnN7vQn29j8VOELA" alt=""><figcaption><p><strong>DGV Gold</strong> track</p></figcaption></figure>

## Decipher Healthy Population

The **Decipher Healthy Population** track displays variants observed in healthy individuals from the Deciphering Developmental Disorders study.

Use it to compare findings against a baseline of unaffected genomes.

<figure><img src="/files/jyU7LuxpiXGDIKQsqOCc" alt=""><figcaption><p><strong>Decipher Healthy Population</strong> track</p></figcaption></figure>


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