A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942620



Internal ID22718061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47800616..47818218hg38UCSC Ensembl
chr16:47834527..47852129hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3817603
hg1917603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942620
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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