A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031784



Internal ID20598824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69358290..69359751hg38UCSC Ensembl
chr16:69392193..69393654hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381462
hg191462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503871
Supporting Variants
Samples
Known GenesTERF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031784
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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