A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145534



Internal ID344739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81866385..81866669hg38UCSC Ensembl
chr16:81899990..81900274hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709878
Samples
Known GenesPLCG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145534
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer