A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986282



Internal ID21895625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:137777438..137780272hg38UCSC Ensembl
chr2:138535008..138537842hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg382835
hg192835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517977
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986282
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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