A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647811



Internal ID21839858
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 StatusS
Merged Variantsnsv6045616
Supporting Variants
Samples
Known GenesTMEM184B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647811
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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