A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911774



Internal ID22686989
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 StatusM
Merged Variants
Supporting Variantsnssv17355305
Samples
Known GenesCUL5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911774
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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