A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4165155



Internal ID20037410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99962421..100028327hg38UCSC Ensembl
chr7:99560044..99625950hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3865907
hg1965907
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15981910
Samples
Known GenesAZGP1, AZGP1P1, ZKSCAN1
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)nsv4165155
Frequency
Sample Size10847
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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