A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1636e59



Internal ID22762856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:72059952..72078350hg38UCSC Ensembl
chr16:72093851..72112249hg19UCSC Ensembl
chr16:70651352..70669750hg18UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3818399
hg1918399
hg1818399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3386036, esv3443812
SamplesNA19238, NA19240
Known GenesHP, HPR
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1636e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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