A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658116



Internal ID9924221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87113126..87121424hg38UCSC Ensembl
Outerchr16:87113089..87121474hg38UCSC Ensembl
Innerchr16:87146732..87155030hg19UCSC Ensembl
Outerchr16:87146695..87155080hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg388386
hg198386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6513377
SamplesNA19379
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658116
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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