A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4944n223



Internal ID22807912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94893701..94945500hg38UCSC Ensembl
chr3:94612545..94664344hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3851800
hg1951800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6360195, nsv6373945
Samples
Known GenesLINC00879
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4944n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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