A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900899



Internal ID22676046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39414146..39414309hg38UCSC Ensembl
chr3:39455637..39455800hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425690
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900899
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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