A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907331



Internal ID22682538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97771552..97780403hg38UCSC Ensembl
chr3:97490396..97499247hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg388852
hg198852
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422098
Samples
Known GenesARL6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907331
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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