A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053716



Internal ID21962949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38229609..38230236hg38UCSC Ensembl
chr22:38625615..38626242hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646636
Samples
Known GenesTMEM184B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053716
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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