A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659314



Internal ID9578733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11429709..11506260hg38UCSC Ensembl
chr16:11523565..11600116hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3876552
hg1976552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5714119
SamplesNA19076
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659314
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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