A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181161



Internal ID20748201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117966365..117967787hg38UCSC Ensembl
chr11:117837080..117838502hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381423
hg191423
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468879
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181161
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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