A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15947397



Internal ID19672651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65492029..65551029hg38UCSC Ensembl
chr11:65259500..65318500hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3859001
hg1959001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4207263
Supporting Variants
Samples
Known GenesLTBP3, MALAT1, MIR548AR, MIR548BA, SCYL1
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)nssv15947397
Frequency
Sample Size10847
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000047


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