A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17524566



Internal ID21848924
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 StatusS
Merged Variantsnsv5991160
Supporting Variants
Samples
Known GenesLYG2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17524566
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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