A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900033



Internal ID22675171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165700702..165741575hg38UCSC Ensembl
chr2:166557212..166598085hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3840874
hg1940874
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406268
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900033
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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