A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4095544



Internal ID20333752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133267..313211hg38UCSC Ensembl
chr4:127000..307000hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38179945
hg19180001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15887122
Samples
Known GenesZNF718, ZNF732, ZNF876P
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)nsv4095544
Frequency
Sample Size10847
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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