A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193274



Internal ID20760314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10395548..10407423hg38UCSC Ensembl
chr11:10417095..10428970hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811876
hg1911876
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439467
Supporting Variants
Samples
Known GenesCAND1.11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193274
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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