A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988619



Internal ID21897962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25228199..25228251hg38UCSC Ensembl
chr2:25451068..25451120hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520785
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988619
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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