A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15967026



Internal ID19692280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197016..655135hg38UCSC Ensembl
chr2:197016..655135hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38458120
hg19458120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4068442
Supporting Variants
Samples
Known GenesACP1, FAM150B, SH3YL1
MethodSequencing
AnalysisSV calls were generated using multi-algorithm consensus pipeline involving raw evidence assessment, filtering, clustering, genotyping, alternative allele structure resolution, and gene annotation. These methods are described in detail in the gnomAD-SV preprint [Collins*, Brand*, et al., bioRxiv (2019)|https://www.biorxiv.org/content/10.1101/578674v1], and are largely based on methods developed in [Werling et al., Nat. Genet. (2018)|https://www.ncbi.nlm.nih.gov/pubmed/29700473].
Platform
Comments
ReferencegnomAD_Structural_Variants
Pubmed ID12345678
Accession Number(s)nssv15967026
Frequency
Sample Size10847
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000092


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