A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5653979



Internal ID8631382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:168526..177588hg38UCSC Ensembl
chr18:168526..177588hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg389063
hg199063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675103
Supporting Variants
SamplesHG00732
Known GenesUSP14
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5653979
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