A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941065



Internal ID22716483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13333914..13358610hg38UCSC Ensembl
chr16:13427771..13452467hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3824697
hg1924697
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388225
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941065
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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