A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181322



Internal ID20748362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10878916..11240040hg38UCSC Ensembl
chr11:10900463..11261587hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38361125
hg19361125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449448
Supporting Variants
Samples
Known GenesZBED5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181322
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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