A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208642



Internal ID20775684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41194601..41202400hg38UCSC Ensembl
chr3:41236092..41243891hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372607
Supporting Variants
Samples
Known GenesCTNNB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208642
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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