A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1286n223



Internal ID22804254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97923006..98008548hg38UCSC Ensembl
chr11:97794006..97879276hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3885543
hg1985271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6458012, nsv6463868
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1286n223
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