A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728911



Internal ID152577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38259919..38267533hg38UCSC Ensembl
chr22:38655925..38663539hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg387615
hg197615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551201
Supporting Variants
Samples
Known GenesTMEM184B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728911
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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