A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527164



Internal ID303269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22474177..22487263hg38UCSC Ensembl
chr18:20054140..20067226hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3813087
hg1913087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17716608
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527164
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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