A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668844



Internal ID9934949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68650341..68653273hg38UCSC Ensembl
chr16:68684244..68687176hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382933
hg192933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6249569
SamplesNA19713
Known GenesCDH3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668844
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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