A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928956



Internal ID22704202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81803232..81808606hg38UCSC Ensembl
chr16:81836837..81842211hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg385375
hg195375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374834
Samples
Known GenesPLCG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928956
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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