A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17048538



Internal ID100234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76405505..76413460hg38UCSC Ensembl
chr11:76116549..76124504hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg387956
hg197956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493982
Supporting Variants
Samples
Known GenesLOC100506127
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17048538
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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