A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178365



Internal ID20745405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89064501..89303800hg38UCSC Ensembl
chr16:89130909..89370208hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38239300
hg19239300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497533
Supporting Variants
Samples
Known GenesACSF3, ANKRD11, CDH15, LINC00304, LOC400558, SLC22A31, ZNF778
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178365
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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