A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191521



Internal ID20758561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94613869..94615784hg38UCSC Ensembl
chr11:94347035..94348950hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381916
hg191916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470193
Supporting Variants
Samples
Known GenesPIWIL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191521
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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