A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904259



Internal ID22679435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149195416..149195523hg38UCSC Ensembl
chr3:148913203..148913310hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410506
Samples
Known GenesCP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904259
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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