A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5667316



Internal ID8644719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113935087..113935460hg38UCSC Ensembl
chr11:113805809..113806182hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675456
Supporting Variants
SamplesHG00625
Known GenesHTR3B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5667316
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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