A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5545027



Internal ID319109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37576301..37598053hg38UCSC Ensembl
chr22:37972308..37994060hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3821753
hg1921753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728846
Samples
Known GenesLGALS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5545027
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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