A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659746



Internal ID9925851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:30072016..30074045hg38UCSC Ensembl
Outerchr16:30071859..30074206hg38UCSC Ensembl
Innerchr16:30083337..30085366hg19UCSC Ensembl
Outerchr16:30083180..30085527hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382348
hg192348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5786290
SamplesHG01170
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659746
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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