A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059083



Internal ID107258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84477368..84644628hg38UCSC Ensembl
chr11:84188411..84355671hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38167261
hg19167261
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497144
Supporting Variants
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17059083
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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