A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730504



Internal ID20506416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108900764..108900820hg38UCSC Ensembl
chr9:111663044..111663100hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277426
Samples
Known GenesIKBKAP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730504
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