A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4133664



Internal ID20014565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10671423..11457218hg38UCSC Ensembl
chr7:10711050..11496845hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38785796
hg19785796
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2303n166
Supporting Variantsnssv15980331
Samples
Known GenesNDUFA4, PHF14, THSD7A
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)nsv4133664
Frequency
Sample Size10847
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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