A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966302



Internal ID22741237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40720281..40720497hg38UCSC Ensembl
chr22:41116285..41116501hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408065
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966302
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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