A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182474



Internal ID20749514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84291354..84425805hg38UCSC Ensembl
chr11:84002397..84136848hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38134452
hg19134452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455730
Supporting Variants
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182474
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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