A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369345



Internal ID22595014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124208803..124225727hg38UCSC Ensembl
chr11:124079510..124096432hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3816925
hg1916923
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907917
Supporting Variants
Samples
Known GenesOR8G2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369345
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005


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