A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17399226



Internal ID22457096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16842539..16856097hg38UCSC Ensembl
chr2:17023806..17037364hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3813559
hg1913559
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885610
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17399226
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007


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