A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5840994



Internal ID9048257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61945681..61961287hg38UCSC Ensembl
chr16:61979585..61995191hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3815607
hg1915607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677187
Supporting Variants
SamplesHG00692
Known GenesCDH8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5840994
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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