A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4276734



Internal ID20114961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22899195..23319697hg38UCSC Ensembl
chr20:22879833..23300334hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38420503
hg19420502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15965481
Samples
Known GenesCD93, LINC00656, SSTR4, THBD
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)nsv4276734
Frequency
Sample Size10847
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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