A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742535



Internal ID20518519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9822720..9822777hg38UCSC Ensembl
chr3:9864404..9864461hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295816
Samples
Known GenesARPC4-TTLL3, TTLL3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742535
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