A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903041



Internal ID22678205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13123923..13136210hg38UCSC Ensembl
chr3:13165423..13177710hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3812288
hg1912288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903041
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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