A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739960



Internal ID20515935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133105811..133105868hg38UCSC Ensembl
chr9:135981198..135981255hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275762
Samples
Known GenesRALGDS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739960
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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