A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4032998



Internal ID20163886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8547567..8556267hg38UCSC Ensembl
chr21:9436400..9445100hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg388701
hg198701
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15781511, nssv15781516, nssv15781514, nssv15781513, nssv15781510, nssv15781509, nssv15781517, nssv15781508, nssv15781512, nssv15781515
Samples
Known Genes
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)nsv4032998
Frequency
Sample Size10847
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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