A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1664e59



Internal ID20128413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89137143..89137841hg38UCSC Ensembl
chr16:89203551..89204249hg19UCSC Ensembl
chr16:87731052..87731750hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38699
hg19699
hg18699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3444909, esv3419079
SamplesNA19239, NA19240
Known GenesACSF3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1664e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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