A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959194



Internal ID22734233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:22441834..22441834hg38UCSC Ensembl
chr3:22483325..22483325hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959194
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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