A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045893



Internal ID98385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24944661..24967888hg38UCSC Ensembl
chr11:24966207..24989434hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3823228
hg1923228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501683
Supporting Variants
Samples
Known GenesLUZP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045893
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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