A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663529



Internal ID9929634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81418265..81427590hg38UCSC Ensembl
Outerchr16:81418228..81427640hg38UCSC Ensembl
Innerchr16:81451870..81461195hg19UCSC Ensembl
Outerchr16:81451833..81461245hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg389413
hg199413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6512063
SamplesHG00258
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663529
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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