A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902186



Internal ID22677341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132172341..132172391hg38UCSC Ensembl
chr3:131891185..131891235hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399973
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902186
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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