A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195405



Internal ID20762445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55809101..55822500hg38UCSC Ensembl
chr16:55843013..55856412hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3813400
hg1913400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513884
Supporting Variants
Samples
Known GenesCES1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195405
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.15344


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