A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760059



Internal ID20535919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135033177..135033177hg38UCSC Ensembl
chr2:135790747..135790747hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292146
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760059
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