A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5552520



Internal ID325865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44423790..44425232hg38UCSC Ensembl
chr22:44819670..44821112hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381443
hg191443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17729401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5552520
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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