A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4192783



Internal ID20057234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4619101..5268941hg38UCSC Ensembl
chr11:4640331..5290171hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38649841
hg19649841
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15952843
Samples
Known GenesHBB, HBBP1, HBD, HBE1, HBG1, HBG2, MMP26, OR51A2, OR51A4, OR51A7, OR51D1, OR51E1, OR51E2, OR51F1, OR51F2, OR51G1, OR51G2, OR51L1, OR51S1, OR51T1, OR51V1, OR52A1, OR52A5, OR52E2, OR52J3, OR52R1
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)nsv4192783
Frequency
Sample Size10847
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer