A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15886560



Internal ID19611814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5676599..5793706hg38UCSC Ensembl
chr4:5678326..5795433hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38117108
hg19117108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4110222
Supporting Variants
Samples
Known GenesEVC, EVC2
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)nssv15886560
Frequency
Sample Size10847
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000046


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