A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764489



Internal ID20540349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116633647..116633647hg38UCSC Ensembl
chr10:118393158..118393158hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268218
Samples
Known GenesPNLIPRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764489
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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