A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519086



Internal ID295441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47177975..47182928hg38UCSC Ensembl
chr16:47211886..47216839hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg384954
hg194954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709357
Samples
Known GenesITFG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519086
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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