A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5622351



Internal ID8599754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18584667..18600238hg38UCSC Ensembl
chr11:18606214..18621785hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3815572
hg1915572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660842
Supporting Variants
SamplesHG01125
Known GenesSPTY2D1-AS1, UEVLD
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5622351
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