A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15788268



Internal ID19513619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59495812..60468567hg38UCSC Ensembl
chr15:59788011..60760766hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38972756
hg19972756
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4344078
Supporting Variants
Samples
Known GenesANXA2, BNIP2, FAM81A, FOXB1, GCNT3, GTF2A2, NARG2
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
Commentscomplex variant
ReferencegnomAD_Structural_Variants
Pubmed ID12345678
Accession Number(s)nssv15788268
Frequency
Sample Size10847
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000092


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer