A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986625



Internal ID21895968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162936686..162937241hg38UCSC Ensembl
chr2:163793196..163793751hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535918
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986625
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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