A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028149



Internal ID20595189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19409674..19410854hg38UCSC Ensembl
chr16:19420996..19422176hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg381181
hg191181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511344
Supporting Variants
Samples
Known GenesTMC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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