A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209198



Internal ID20776238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169763201..169777100hg38UCSC Ensembl
chr3:169480989..169494888hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3813900
hg1913900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373985
Supporting Variants
Samples
Known GenesACTRT3, MYNN, TERC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209198
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00026


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