A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2120n166



Internal ID22802019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37422510..38043992hg38UCSC Ensembl
chr6:37390286..38011768hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38621483
hg19621483
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4124273, nsv4136853
Samples
Known GenesCCDC167, CMTR1, MDGA1, MIR4462, ZFAND3
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 ID32461652
Accession Number(s)dgv2120n166
Frequency
Sample Size10847
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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