A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5348n223



Internal ID22808316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82991601..82999300hg38UCSC Ensembl
chr4:83912754..83920453hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg387700
hg197700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6376252, nsv6388283
Samples
Known GenesLIN54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5348n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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