A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5972603



Internal ID8950006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36455547..36457626hg38UCSC Ensembl
chr18:34035510..34037589hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg382080
hg192080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672452
Supporting Variants
SamplesNA18511
Known GenesFHOD3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5972603
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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