A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4275701



Internal ID20114509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42075707..42200578hg38UCSC Ensembl
chr21:43495816..43620688hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38124872
hg19124873
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15967619
Samples
Known GenesABCG1, C21orf128, UMODL1
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)nsv4275701
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