A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211226



Internal ID20778266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95383001..95405100hg38UCSC Ensembl
chr3:95101845..95123944hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3822100
hg1922100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362633
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211226
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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