A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv995n223



Internal ID22803963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:23727301..23731900hg38UCSC Ensembl
chr11:23748847..23753446hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6435889, nsv6454551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv995n223
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