A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439887



Internal ID218413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133233577..133244665hg38UCSC Ensembl
chr3:132952421..132963509hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3811089
hg1911089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939609
Samples
Known GenesTMEM108
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439887
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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