A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15790411



Internal ID19515784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171596..685845hg38UCSC Ensembl
chr5:171711..685960hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38514250
hg19514250
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4562211
Supporting Variants
Samples
Known GenesAHRR, C5orf55, CCDC127, CEP72, EXOC3, LOC100996325, LOC102467073, LRRC14B, MIR4456, PDCD6, PLEKHG4B, PP7080, SDHA, SLC9A3, TPPP
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)nssv15790411
Frequency
Sample Size10847
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000138


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