A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988162



Internal ID21897505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223608382..223608616hg38UCSC Ensembl
chr2:224473100..224473334hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988162
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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