A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1834e59



Internal ID22763054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83026287..83027085hg38UCSC Ensembl
chr17:80984163..80984961hg19UCSC Ensembl
chr17:78577452..78578250hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38799
hg19799
hg18799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3347307, esv3435541
SamplesNA19239, NA19240
Known GenesB3GNTL1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1834e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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