A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678609



Internal ID9944714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27065742..27087457hg38UCSC Ensembl
Outerchr16:27065705..27087507hg38UCSC Ensembl
Innerchr16:27077063..27098778hg19UCSC Ensembl
Outerchr16:27077026..27098828hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3821803
hg1921803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6504593
SamplesNA18606
Known GenesC16orf82
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678609
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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