A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209698



Internal ID20776738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146082001..146084400hg38UCSC Ensembl
chr3:145799788..145802187hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369607
Supporting Variants
Samples
Known GenesPLOD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209698
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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