A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930990



Internal ID22706266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68979392..68981372hg38UCSC Ensembl
chr16:69013295..69015275hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381981
hg191981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373374
Samples
Known GenesTANGO6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930990
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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