A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682289



Internal ID21204150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194348284..194348335hg38UCSC Ensembl
chr3:194069013..194069064hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807026
Supporting Variants
Samples
Known GenesCPN2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682289
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.71875


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