A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991160



Internal ID21900503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:99251908..99252124hg38UCSC Ensembl
chr2:99868371..99868587hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524566
Samples
Known GenesLYG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991160
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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