A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664110



Internal ID21612415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81704694..81704694hg38UCSC Ensembl
chr16:81738299..81738299hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084459
SamplesHG03371
Known GenesCMIP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664110
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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