A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910140



Internal ID7536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:18141692..18164861hg38UCSC Ensembl
chr2:18322958..18346127hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3823170
hg1923170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139944
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910140
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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