A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663777



Internal ID9929882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31174123..31175230hg38UCSC Ensembl
Outerchr16:31174086..31175280hg38UCSC Ensembl
Innerchr16:31185444..31186551hg19UCSC Ensembl
Outerchr16:31185407..31186601hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381195
hg191195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5419372, essv5575732
SamplesNA18985, NA18632
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663777
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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