A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897786



Internal ID22672893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190144669..190144719hg38UCSC Ensembl
chr3:189862458..189862508hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897786
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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