A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664327



Internal ID9583746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27325123..27339759hg38UCSC Ensembl
Outerchr16:27324961..27339914hg38UCSC Ensembl
Innerchr16:27336444..27351080hg19UCSC Ensembl
Outerchr16:27336282..27351235hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3814954
hg1914954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5474687, essv6375498, essv5827117, essv5669026, essv6106734
SamplesHG00112, HG00117, HG00324, HG00143, HG00336
Known GenesIL4R
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664327
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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