A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5980934



Internal ID9106937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21715659..21715841hg38UCSC Ensembl
chr22:22069948..22070130hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678585
Supporting Variants
SamplesHG01101
Known GenesYPEL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5980934
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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