A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986156



Internal ID21895499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:138093063..138205147hg38UCSC Ensembl
chr2:138850633..138962717hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38112085
hg19112085
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986156
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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