A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678036



Internal ID9944141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31824759..31830504hg38UCSC Ensembl
Outerchr16:31824717..31830558hg38UCSC Ensembl
Innerchr16:31836080..31841825hg19UCSC Ensembl
Outerchr16:31836038..31841879hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg385842
hg195842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5493150
SamplesNA06989
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678036
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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