A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663065



Internal ID9929170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30169842..30170046hg38UCSC Ensembl
chr22:30565831..30566035hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5568731
SamplesNA19093
Known GenesHORMAD2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663065
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