A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031707



Internal ID20598747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68458131..68486395hg38UCSC Ensembl
chr16:68492034..68520298hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3828265
hg1928265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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