A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516362



Internal ID292821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68312292..68312894hg38UCSC Ensembl
chr16:68346195..68346797hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38603
hg19603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707560
Samples
Known GenesPRMT7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516362
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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