A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962898



Internal ID22737833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145556824..145556824hg38UCSC Ensembl
chr3:145274611..145274611hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406810
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962898
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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