A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196664



Internal ID20763704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39763596..39767879hg38UCSC Ensembl
chr11:39785146..39789429hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg384284
hg194284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196664
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00043


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