A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1655e59



Internal ID22762875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87124045..87125443hg38UCSC Ensembl
chr16:87157651..87159049hg19UCSC Ensembl
chr16:85715152..85716550hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3445172, esv3369561, esv3382372
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1655e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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