A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355305



Internal ID22580974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108099164..108119362hg38UCSC Ensembl
chr11:107969891..107990089hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3820199
hg1920199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911774
Supporting Variants
Samples
Known GenesCUL5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355305
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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