A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209196



Internal ID20776236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169762301..169777000hg38UCSC Ensembl
chr3:169480089..169494788hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3814700
hg1914700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367562
Supporting Variants
Samples
Known GenesACTRT3, MYNN, TERC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209196
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00033


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