A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425491



Internal ID22483361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:166803358..166816462hg38UCSC Ensembl
chr3:166521146..166534250hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3813105
hg1913105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892503
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425491
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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