A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661660



Internal ID9927765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68457281..68458088hg38UCSC Ensembl
chr16:68491184..68491991hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6121752, essv6091762
SamplesNA19058, NA18576
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661660
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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