A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411724



Internal ID22469594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20450103..20570979hg38UCSC Ensembl
chr3:20491595..20612471hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38120877
hg19120877
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901922
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411724
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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