A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1833e59



Internal ID22763053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83022087..83023385hg38UCSC Ensembl
chr17:80979963..80981261hg19UCSC Ensembl
chr17:78573252..78574550hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381299
hg191299
hg181299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3348459, esv3419369, esv3451466
SamplesNA19238, NA19239, NA19240
Known GenesB3GNTL1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1833e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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