A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748203



Internal ID20524228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98155633..98212354hg38UCSC Ensembl
chr3:97874477..97931198hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3856722
hg1956722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286976
Samples
Known GenesOR5H15
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748203
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