A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988821



Internal ID21898164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25994460..25998585hg38UCSC Ensembl
chr2:26217329..26221454hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg384126
hg194126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988821
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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