A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765012



Internal ID20540872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122563428..122563428hg38UCSC Ensembl
chr8:123575667..123575667hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg385906
hg195906
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765012
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