A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502684



Internal ID279543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2300085..2330106hg38UCSC Ensembl
chr11:2321315..2351336hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3830022
hg1930022
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043603
Samples
Known GenesC11orf21, CD81-AS1, TSPAN32
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502684
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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