A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16911008



Internal ID8108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25674845..25694016hg38UCSC Ensembl
chr2:25897714..25916885hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3819172
hg1919172
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16911008
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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