A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661622



Internal ID9927727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46397323..46464992hg38UCSC Ensembl
Outerchr16:46397289..46465027hg38UCSC Ensembl
Innerchr16:46431235..46498904hg19UCSC Ensembl
Outerchr16:46431201..46498939hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3867739
hg1967739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv494e199
Supporting Variantsessv5956226
SamplesNA19764
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661622
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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