A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210538



Internal ID20777578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33405488..33407651hg38UCSC Ensembl
chr3:33446980..33449143hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg382164
hg192164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373526
Supporting Variants
Samples
Known GenesUBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210538
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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