A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181076



Internal ID20748116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102451301..102453400hg38UCSC Ensembl
chr11:102322032..102324131hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467331
Supporting Variants
Samples
Known GenesTMEM123
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181076
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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