A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192343



Internal ID20759383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55808101..55820200hg38UCSC Ensembl
chr16:55842013..55854112hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3812100
hg1912100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504479
Supporting Variants
Samples
Known GenesCES1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192343
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.15365


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