A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988636



Internal ID21897979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27366028..27366185hg38UCSC Ensembl
chr2:27588895..27589052hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534363
Samples
Known GenesEIF2B4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988636
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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