A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208669



Internal ID20775711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43281401..43294000hg38UCSC Ensembl
chr3:43322893..43335492hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3812600
hg1912600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359125
Supporting Variants
Samples
Known GenesSNRK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208669
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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