A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17054483



Internal ID104157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132339724..132384882hg38UCSC Ensembl
chr11:132209618..132254776hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3845159
hg1945159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494349
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17054483
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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