A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666789



Internal ID9932894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:29706810..29711428hg38UCSC Ensembl
Outerchr16:29706773..29711478hg38UCSC Ensembl
Innerchr16:29718131..29722749hg19UCSC Ensembl
Outerchr16:29718094..29722799hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg384706
hg194706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5652132
SamplesHG01174
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666789
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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