A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093549



Internal ID20660589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119873932..119874246hg38UCSC Ensembl
chr3:119592779..119593093hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365836
Supporting Variants
Samples
Known GenesGSK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093549
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00161


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