A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389582



Internal ID22447452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1588239..1593359hg38UCSC Ensembl
chr16:1638240..1643360hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385121
hg195121
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937315
Supporting Variants
Samples
Known GenesIFT140
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389582
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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