A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419900



Internal ID22477770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26767880..26802639hg38UCSC Ensembl
chr3:26809371..26844130hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3834760
hg1934760
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5888400
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419900
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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