A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045616



Internal ID21954880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38256518..38258450hg38UCSC Ensembl
chr22:38652524..38654456hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381933
hg191933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647811
Samples
Known GenesTMEM184B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045616
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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