A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755793



Internal ID20531653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3074615..3074615hg38UCSC Ensembl
chr4:3076342..3076342hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278502
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755793
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