A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045603



Internal ID98166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32562486..32591140hg38UCSC Ensembl
chr11:32584032..32612686hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3828655
hg1928655
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501313
Supporting Variants
Samples
Known GenesEIF3M
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045603
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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