A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5844620



Internal ID8822023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66487242..66488760hg38UCSC Ensembl
chr16:66521145..66522663hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381519
hg191519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672892
Supporting Variants
SamplesNA19452
Known GenesBEAN1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5844620
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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