A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5609001



Internal ID8586404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35064792..35171579hg38UCSC Ensembl
Outerchr22:35064758..35171614hg38UCSC Ensembl
Innerchr22:35460785..35567572hg19UCSC Ensembl
Outerchr22:35460751..35567607hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38106857
hg19106857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661366
Supporting Variants
SamplesNA18612
Known GenesISX
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5609001
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