A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211396



Internal ID20778436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148868584..148879996hg38UCSC Ensembl
chr3:148586371..148597783hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3811413
hg1911413
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357279
Supporting Variants
Samples
Known GenesCPA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211396
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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