A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962831



Internal ID22737766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31974328..31976410hg38UCSC Ensembl
chr22:32370315..32372397hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382083
hg192083
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396144
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962831
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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