A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5778302



Internal ID9785116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18455226..18455832hg38UCSC Ensembl
chr19:18566036..18566642hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2657907
Supporting Variants
SamplesNA19776
Known GenesELL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5778302
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