A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv111n223



Internal ID22803079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20079901..20084194hg38UCSC Ensembl
chr1:20406394..20410687hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg384294
hg194294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6329304, nsv6323681
Samples
Known GenesPLA2G5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv111n223
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