A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1828e59



Internal ID22763048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80510857..80512055hg38UCSC Ensembl
chr17:78484657..78485855hg19UCSC Ensembl
chr17:76099252..76100450hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3432388, esv3352240
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1828e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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