A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178652



Internal ID20745692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102181345..102183892hg38UCSC Ensembl
chr11:102052076..102054623hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382548
hg192548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459289
Supporting Variants
Samples
Known GenesYAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178652
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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