A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372320



Internal ID22597989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79857039..79893623hg38UCSC Ensembl
chr16:79890936..79927520hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3836585
hg1936585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5941369
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372320
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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