A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179422



Internal ID20746462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115505934..115511999hg38UCSC Ensembl
chr11:115376652..115382717hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg386066
hg196066
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459590
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179422
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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