A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910640



Internal ID7867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27068399..27068461hg38UCSC Ensembl
chr2:27291267..27291329hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434693
Supporting Variants
Samples
Known GenesAGBL5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910640
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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