A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185787



Internal ID20752827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44799513..44831278hg38UCSC Ensembl
chr11:44821063..44852829hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3831766
hg1931767
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467900
Supporting Variants
Samples
Known GenesTSPAN18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185787
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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