A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950158



Internal ID22725570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34549728..34557945hg38UCSC Ensembl
chr22:34945720..34953937hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg388218
hg198218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402613
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950158
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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