A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765996



Internal ID20541856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76974453..76974453hg38UCSC Ensembl
chr5:76270278..76270278hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765996
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