A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4521752



Internal ID19905182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185395210..186031211hg38UCSC Ensembl
chr3:185112998..185749000hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38636002
hg19636003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15970083
Samples
Known GenesC3orf65, IGF2BP2, LIPH, LOC344887, MAP3K13, SENP2, TMEM41A, TRA2B
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)nsv4521752
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