A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209410



Internal ID20776450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:790010..3040518hg38UCSC Ensembl
chr3:831693..3082202hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg382250509
hg192250510
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360651
Supporting Variants
Samples
Known GenesCNTN4, CNTN4-AS2, CNTN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209410
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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