A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528769



Internal ID304813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69875943..69889727hg38UCSC Ensembl
chr18:67543179..67556963hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3813785
hg1913785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719203
Samples
Known GenesCD226
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528769
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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