A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051738



Internal ID102334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133650021..133650074hg38UCSC Ensembl
chr11:133519916..133519969hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5508202
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051738
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.547924


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