A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3352116



Internal ID15199097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70151048..70153846hg38UCSC Ensembl
Innerchr16:70152048..70152846hg38UCSC Ensembl
Outerchr16:70150048..70154846hg38UCSC Ensembl
chr16:70184951..70187749hg19UCSC Ensembl
Innerchr16:70185951..70186749hg19UCSC Ensembl
Outerchr16:70183951..70188749hg19UCSC Ensembl
chr16:68742452..68745250hg18UCSC Ensembl
Innerchr16:68743452..68744250hg18UCSC Ensembl
Outerchr16:68741452..68746250hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382799
hg192799
hg182799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1626e59
Supporting Variantsessv8690415
SamplesNA19239
Known GenesPDPR
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3352116
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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