A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986034



Internal ID21895377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13396290..14199761hg38UCSC Ensembl
chr2:13536415..14339885hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38803472
hg19803471
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986034
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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