A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665628



Internal ID9585047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:193183..193837hg38UCSC Ensembl
chr16:243182..243836hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5555377, essv5416712, essv5708832, essv6458604, essv6562547, essv5845594, essv5771473, essv6326738
SamplesNA19819, NA20808, NA19404, NA19471, NA19391, NA19338, NA19398, NA19248
Known GenesLUC7L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665628
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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