A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962800



Internal ID22737735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4878894..4878894hg38UCSC Ensembl
chr3:4920578..4920578hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425708
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962800
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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