A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4069661



Internal ID20314663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:248567699..248634899hg38UCSC Ensembl
chr1:248731000..248798200hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3867201
hg1967201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15850666
Samples
Known GenesOR2T10, OR2T11, OR2T34
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)nsv4069661
Frequency
Sample Size10847
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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