A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6357744



Internal ID9335147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72637009..72637152hg38UCSC Ensembl
chr11:72348053..72348196hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664373
Supporting Variants
SamplesNA18873
Known GenesPDE2A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6357744
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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