A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422098



Internal ID22479968
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 StatusS
Merged Variantsnsv5907331
Supporting Variants
Samples
Known GenesARL6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422098
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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