A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5776774



Internal ID9885337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38155214..38162192hg38UCSC Ensembl
Outerchr22:38155177..38162242hg38UCSC Ensembl
Innerchr22:38551221..38558199hg19UCSC Ensembl
Outerchr22:38551184..38558249hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg387066
hg197066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661596
Supporting Variants
SamplesNA20760
Known GenesPLA2G6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5776774
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